Posted on July 9, 2022 by Recalls Direct™

![Canadian Tire Paderno Glass Square Baking Dishes Recall [Canada]](https://livingsafelyrecalls.files.wordpress.com/2022/07/15996-canadian-tire-paderno-glass-square-baking-dishes.jpg?w=96&h=81)
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Canada/Ottawa: Canadian Tire Corporation Limited, a Toronto, Ontario establishment, recalls an estimated 10,800 Paderno branded Glass Square Baking Dishes with Lids from the Canadian marketplace due to reported operational breakage upon extreme temperature exposure and consequential risks of consequential risks of laceration, eye damage, concussion, bone fractures and/or central nervous system (“CNS”) injury, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.
HCSC: https://bit.ly/3uArOQx
Direct link: https://recalls-rappels.canada.ca/en/alert-recall/paderno-17-qt-glass-square-baking-dish-lid-recalled-due-injury-hazards
Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Glass Square Baking Dishes are subject to this recall: Continue reading →
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Filed under: Assistive, health or safety devices, Health Canada/Santé Canada, Home & Residential, Vehicles | Tagged: Canadian Tire Corporation Limited, HCSC ID number: RA-64322, Health Canada, kitchen, Laceration hazard, operational failure hazard, Paderno, Paderno branded Glass Square Baking Dishes, Recalls Direct RIN: 15996-2022, Santé Canada, Traumatic Brain Injury hazard | Leave a comment »
Posted on June 24, 2022 by Recalls Direct™
Washington, DC:
As of Friday, June 24, 2022, the US National Highway Traffic Safety Administration (“NHTSA”), a division of the US Department of Transportation, has posted a total of sixty-eight (68) vehicle, tire, accessory or other automotive-related product recalls this month.
Are yours listed? http://ht.ly/cXy430qH5Ln
Direct link: https://www.nhtsa.gov/search/safety-issues#recall
Additional information:
Among the sixty-two (62) recalls the NHTSA has announced this June comes news of the following:
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Filed under: Assistive, health or safety devices, crash hazard, US NHTSA, Vehicles | Tagged: 22E047000, Bendix Commercial Vehicle Systems, crash hazard, loss of vehicle control hazard, NHTSA Campaign Number: 22E047000, operational failure hazard, R.H. Sheppard, Recalls Direct RIN: 15931-2022, Steering Gear malfunction, US National Highway Traffic Safety Administration, US NHTSA | Leave a comment »
Posted on June 15, 2022 by Recalls Direct™

![Princess Auto Multi-Function Emergency Tools Recall [Canada]](https://livingsafelyrecalls.files.wordpress.com/2022/06/15906-princess-auto-multi-function-emergency-tools.jpg?w=124&h=42)
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Canada/Ottawa: Princess Auto Limited, a Winnipeg, Manitoba establishment, recalls an estimated 197 Multi-Function Emergency Tools from the Canadian marketplace due to suspected operational failure during an emergency and consequential risks of entrapment and/or injury in the event of a crash, motor vehicle collision (“MVC”) or other impact event, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.
HCSC: https://cutt.ly/HJ5IzWS
Direct link: https://recalls-rappels.canada.ca/en/alert-recall/multi-function-emergency-tool-recalled-due-potential-product-failure-during-emergency
Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Emergency Tools are subject to this recall:
Continue reading →
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Filed under: Assistive, health or safety devices, Health Canada/Santé Canada, Home & Residential, Vehicles | Tagged: assistive, Flashlight, HCSC ID number: RA-64250, Health Canada, Multi-Function Emergency Tool, operational failure hazard, Princess Auto Limited, Princess Auto Multi-Function Emergency Tools, Recalls Direct RIN: 15906-2022, Santé Canada, Seat Belt Cutter, Torch Light, Window Breaker | Leave a comment »
Posted on April 11, 2022 by Recalls Direct™
![USI 2-in-1 Photoelectric Smoke & Fire + Carbon Monoxide Alarms Recall [US]](https://livingsafelyrecalls.files.wordpress.com/2022/04/15675-usi-photoelectric-smoke-fire-carbon-monoxide-alarms.jpg?w=96&h=97)
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US/Washington: Universal Security Instruments Inc., an Owings Mills, Maryland establishment, recalls an estimated 8,000 USI 2-in-1 Photoelectric Smoke & Fire + Carbon Monoxide Alarms from the American marketplace due to suspected operation failure and consequential risks of Carbon Monoxide poisoning, smoke inhalation, respiratory failure and cardiac system collapse, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.
CPSC: http://ht.ly/KOZY30sh3hw
Direct link: https://www.cpsc.gov/Recalls/2022/Universal-Security-Instruments-Recalls-Combination-Photoelectric-Smoke-Carbon-Monoxide-Alarms-Due-to-Risk-of-Failure-to-Alert-Consumers-to-Hazardous-Levels-of-Carbon-Monoxide
Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves two (2) models and two (2) date codes of Universal Security Instruments 2-in-1 Photoelectric Smoke & Fire + Carbon Monoxide Alarms marketed, sold and delivered in the United States, as follows: Continue reading →
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Filed under: Burn or scald hazard, Carbon monoxide inhalation hazard, Fire or smoke hazard, Home & Residential, smoke inhalation hazard, US CPSC | Tagged: burn hazard, carbon monoxide hazard, CPSC recall number: 22-111, operational failure hazard, Recalls Direct RIN: 15675-2022, Smoke Alarm, smoke inhalation hazard, Universal Security Instruments 2-in-1 Photoelectric Smoke & Fire + Carbon Monoxide Alarms, Universal Security Instruments Inc., US Consumer Product Safety Commission | Leave a comment »
Posted on October 10, 2021 by Recalls Direct™

![Bayer Tinactin Powder Spray Recall [Canada]](https://livingsafelyrecalls.files.wordpress.com/2021/10/14992-bayertinactinpowderspray.jpg?w=96&h=128)
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Canada/Ottawa: Bayer Inc., a Mississauga, Ontario establishment, recalls certain batch/lots of Tinactin branded Chill Deodorant Powder Spray, Tinactin branded Aerosol Powder and Tinactin branded Chill Liquid Spray from the Canadian marketplace due to suspected Benzene contamination and consequential risks of Cancers of the Blood and Blood-Forming Tissues, including the Bone Marrow and the Lymphatic System including Leukemia, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-changing injury.
HCSC: http://ht.ly/81XR30rWzEo
Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/76575r-eng.php
Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Tinactin Chill Deodorant Powder Spray products are subject to this recall:
Continue reading →
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Filed under: Health Canada/Santé Canada, Home & Residential, Labeling or regulatory issues, Medical / Veterinary, potentially harmful or lethal ingredients | Tagged: Athlete's Foot treatment, Bayer Inc., Benzene contamination hazard, Cancer hazard, HCSC ID number: RA-76575, Health Canada, operational failure hazard, Recalls Direct RIN: 14992-2021, Santé Canada, Tinactin, Tinactin Aerosol Powder, Tinactin Chill Deodorant Powder Spray, Tinactin Chill Liquid Spray | Leave a comment »
Posted on June 23, 2021 by Recalls Direct™

![Puricia Hand Sanitizer Recall [Canada]](https://livingsafelyrecalls.files.wordpress.com/2021/06/14599-puriciahandsanitizer.jpg?w=125&h=109)
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Canada/Ottawa: Pharmaberg Inc., a Delta, British Columbia establishment, recalls certain batch/lots of Puricia Hand Sanitizer products from the Canadian marketplace due to reported undeclared impurities as well as Benzene and Methanol contamination at elevated levels with consequential risks of operational ineffectiveness, failure to prevent microbial spread and possible bacterial and/or viral contamination, all serious health and safety hazards.
HCSC: http://ht.ly/cOx430rLD7t
Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/75845r-eng.php
Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Hand Sanitizer products are subject to this recall:
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Filed under: Health Canada/Santé Canada, Home & Residential, Labeling or regulatory issues, Medical / Veterinary, potentially harmful or lethal ingredients | Tagged: antiseptic, bacterial contamination hazard, COVID-19, excessive Benzene hazard, hand sanitizer, HCSC ID number: RA-75845, Health Canada, operational failure hazard, Pharmaberg Inc., Recalls Direct RIN: 14599-2021, sanitizer, Santé Canada, undeclared methanol hazard, viral contamination hazard | Leave a comment »
Posted on March 3, 2020 by Recalls Direct™
Australia/Canberra:
Air Liquide Healthcare Pty Ltd, a Melbourne, Victoria establishment, recalls certain batch/lots of Inogen One G3 Concentrator Portable Lightweight Medical Oxygen Machines from the Australian marketplace due to suspected operational failure and consequential risk of oxygen supply loss, asphyxiation and death, all serious health and safety hazards.
ACCC: http://ht.ly/tq9D30qmtPY
Direct link: https://www.productsafety.gov.au/recall/air-liquide-healthcare-pty-ltd-inogen-one-g3-concentrator
Additional information:
The Australian Competition & Consumer Commission (“ACCC”) reports the following At Home Oxygen Equipment products are subject to this recall:
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Filed under: ACCC, Assistive, health or safety devices, Medical / Veterinary, Portable Oxygen Concentrators | Tagged: ACCC, ACCC PRA number: 2020/18229, Air Liquide Healthcare Pty Ltd, asphyxiation hazard, Australian Competition & Consumer Commission, Inogen One, Inogen One G3 Concentrator Portable Lightweight Medical Oxygen Machines, medical equipment, operational failure hazard, POC, Recalls Direct RIN: 12749-2020 | Leave a comment »
Posted on June 18, 2019 by Recalls Direct™

![ZOLL AED Pro External Defibillator Recall [Canada]](https://livingsafelyrecalls.files.wordpress.com/2019/06/11640-zollaedproexternaldefibillators.jpg?w=160&h=119)
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Canada/Ottawa: ZOLL Medical Corporation, a Chelmsford, Massachusetts establishment, recalls an unknown number of ZOLL AED Pro External Defibrillators due to suspected component malfunction and consequential risk of operational failure and possible death during a cardiac event requiring defibrillation, all serious health hazards.
HCSC: http://ht.ly/gPNK30oXwCG
Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/70221r-eng.php
Additional information:
Health Canada/Santé Canada (“HCSC”) reports the following Defibillator products are subject to this recall:
Continue reading →
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Filed under: Assistive, health or safety devices, Death hazard, Defibrillators, Electronics, Health Canada/Santé Canada, Home & Residential, Labeling or regulatory issues, Medical / Veterinary, Work or Industrial Equipment | Tagged: death hazard, defibrillator, HCSC ID number: RA-70221, Health Canada, medical device, operational failure hazard, Recalls Direct RIN: 11640-2019, Santé Canada, ZOLL Medical Corporation | Leave a comment »
Posted on May 30, 2018 by Recalls Direct™
US/Silver Spring:
Allergan plc, an Irvine, California establishment, recalls certain batch/lots of Taytulla Softgel Contraceptive (Birth Control) Capsules due to suspected presence of out-of-sequence Capsules and consequential risk of contraceptive failure and unintended pregnancy, all serious health and safety hazards.
FDA: http://ht.ly/oH2X30kfHEh
Direct link: https://www.fda.gov/Safety/Recalls/ucm609044.htm
Additional information:
The US Food and Drug Administration (“FDA”) reports the following Contraceptive Capsules are subject to this recall:
Continue reading →
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Filed under: Assistive, health or safety devices, Drugs, Labeling or regulatory issues, oral contraceptives, Taytulla, US FDA | Tagged: Allergan, drug, FDA, operational failure hazard, Recalls Direct RIN: 10239-2018, suspected Contraceptive failure hazard, Taytulla, Taytulla Softgel Contraceptive | Leave a comment »
Posted on August 28, 2017 by Recalls Direct™
Belgium/Brussels: The European Union issues Report 34-2017 of its Rapid Alert System containing 42 new consumer, automotive and industrial-based product recalls; a must-read for parents, caregivers, drivers, health and safety workers, company owners, supervisors and others: http://ht.ly/gwYD30eIx5f
Direct link: https://ec.europa.eu/consumers/consumers_safety/safety_products/rapex/alerts/?event=main.weeklyOverview&web_report_id=2512&Year=2017
Additional information:
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Filed under: Bacterial or viral contamination, Burn or scald hazard, Carbon monoxide inhalation hazard, Children, Choking or asphyxiation hazard, Clothing & footwear, Electric shock or electrocution, Electronics, Europe's REACH Regulations, European Union Recalls ("RAPEX"), Fire or smoke hazard, Flammability, Home & Residential, Laceration hazard, Sports equipment, Toys, Vehicles, Work or Industrial Equipment | Tagged: baby car seat, children, EU Recalls, European Union, European Union Rapid Alert "Rapex" Report: 34-2017, European's REACH Regulation, infant car seats, infants, injury hazard, operational failure hazard, Recalls, Recalls Direct RIN: 9130-2017, Vehicles | Leave a comment »
Posted on January 14, 2017 by Recalls Direct™

US/Silver Spring:
Physio-Control issues a Voluntary Field Action for all current Lifepak 1000 Defibrillators due to suspected operational failure, unexpectedly shut-down during patient treatment and possible death, a serious health hazard. FDA: http://ht.ly/UI8o3080aAk
Direct link: http://www.fda.gov/Safety/Recalls/ucm537114.htm
Additional information:
The US Food and Drug Administration (“FDA”) reports the following Medical Devices are subject to this Field Action:
Continue reading →
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Filed under: Assistive, health or safety devices, Death hazard, Food & Drink, Medical / Veterinary, US FDA | Tagged: death hazard, FDA, Lifepak 1000 Defibrillators, operational failure hazard, Physio-Control, Recalls Direct RIN: 8127-2017, US Food and Drug Administration | Leave a comment »
Posted on October 27, 2016 by Recalls Direct™

US/Washington:
TUSA recalls an estimated 175 Wrist-Mounted Dive Computers due to risk of operational failure and consequential drowning and decompression sickness hazards. CPSC: http://ht.ly/qBqs305BKJD
Direct link: https://www.cpsc.gov/Recalls/2017/TUSA-Recalls-Diving-Computers
Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain TUSA DC Solar Link IQ1204 Dive Computer.
Continue reading →
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Filed under: Drowning or submersion, Electronics, Home & Residential, Sports equipment, US CPSC | Tagged: CPSC recall number: 17-016, decompression sickness hazard, Diving Equipment, drowning hazard., operational failure hazard, Recalls Direct RIN: 7783-2016, sports equipment, TUSA, Wrist-Mounted Dive Computers | Leave a comment »
Posted on August 27, 2016 by Recalls Direct™

Canada/Ottawa:
Interlogix recalls an estimated 2,500 Wireless Personal Panic Alarms due to operational failure hazard and consequential risk of non-communication in the event of an emergency. HCSC: http://ht.ly/foj1303DEEa
Direct link: http://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2016/59170r-eng.php
Additional information:
Health Canada/Santé Canada (“HCSC”) reports this recall involves certain Interlogix Wireless Personal Panic Devices, models TX-4200-01-1 (white in color with a UPC of 7-82136-72342-7) and TX-4200-01-2 (black in color with a UPC of 7-82136-72343-4).
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Filed under: Assistive, health or safety devices, Electronics, Home & Residential | Tagged: HCSC, HCSC ID number: RA-59170, Health Canada, Interlogix, operational failure hazard, Recalls Direct RIN: 7498-2016, Wireless Personal Panic Alarm | Leave a comment »
Posted on May 30, 2016 by Recalls Direct™

UK/Basildon:
Argos recalls certain batch/lots of Mamas & Papas Car Seats sold due to possible operational failure and consequential child injury hazard. CTSI: http://ht.ly/XGEq300IaB5
Direct link: http://www.tradingstandards.uk/advice/advice-recall-item.cfm?id=316071
Additional information:
The UK Chartered Trading Standards Institute (“CTSI”) reports the following Car Seats are subject to this recall:
Continue reading →
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Filed under: Assistive, health or safety devices, Children, Food & Drink, Listeria monocytogenes [Gram-pos], UK TSI | Tagged: Argos, child injury hazard, ctsi, Mamas & Papas Car Seats, operational failure hazard, Recalls Direct RIN: 7062-2016, TSI, UK Chartered Trading Standards Institute | Leave a comment »
Posted on April 30, 2016 by Recalls Direct™

US/Washington:
Staples recalls an estimated 2,000 due to Back in Motion Office Chairs due to fall and injury hazards. CPSC: http://ht.ly/4nhvJM
Direct link: http://www.cpsc.gov/en/Recalls/2016/Staples-Recalls-Back-in-Motion-Office-Chairs/
Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain Staples and Quill brand Back in Motion Office Chairs.
Continue reading →
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Filed under: Fall hazard, Home & Residential, US CPSC, Work or Industrial Equipment | Tagged: Back in Motion Office Chairs, CPSC, CPSC recall number: 16-144, fall hazard, injury hazard, operational failure hazard, Recalls Direct RIN: 6903-2016, Staples, US Consumer Product Safety Commission | Leave a comment »