Apple iPhone 12 Interference Warning [US]

Apple iPhone 12 Implantable Device Warning

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US FlagUS/Cupertino: Apple Inc., a Cupertino, California establishment, warns Apple iPhone 12 owners and users to keep their phones at least six (6) inches / fifteen (15) cm away from any implantable device such as pacemakers and/or defibrillators due to possible electronic interference, damage and/or operational failure to life-supporting equipment.

Apple: http://ht.ly/DrX230ruBNp

Direct link: https://support.apple.com/en-us/HT211900

Additional information:
Apple reports magnets and radios inside iPhone devices and MagSafe accessories could cause interference with certain medical devices, as follows:

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Sportmix, Nunn Better & ProPac Pet Food Recall [US]

Sportmix, Nunn Better & ProPac Pet Food Recall [US]

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US FlagUS/Silver Spring: Midwestern Pet Foods, Inc., an Evansville, Indiana establishment, recalls all current batch/lots of Dog and Cat Food products made in its Chickasha Oklahoma Operations Facility with corn products due to Aflatoxin levels that exceed acceptable limits for animals, a serious health hazard requiring immediate veterinarian attention.

FDA: http://ht.ly/W1q730rsRNn

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/midwestern-pet-foods-voluntarily-expands-recall-pet-food-aflatoxin-health-risk

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Dog and Cat Food are subject to this recall:

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John Deere Frontier Rotary Tiller Recall [US & Canada]

John Deere Frontier Rotary Tiller Recall [US & Canada]

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US FlagCanada FlagUS/Washington & Canada/Ottawa: Deere & Company, a Moline, Illinois establishment recalls an estimated total 1,880 of Frontier branded Rotary Tillers (approximately 1,740 in the US and approximately 140 in Canada) from the American and Canadian marketplaces due to suspected missing regulatory warning signage on moving parts of the apparatus and consequential risks of laceration, amputation, concussion, bone fractures and/or central nervous system (“CNS”) injury.

CPSC: http://ht.ly/3tzo30rrLpP; HCSC: http://ht.ly/ZIJu30rrLpU

Direct US link: https://www.cpsc.gov/Recalls/2021/John-Deere-Recalls-Frontier-Rotary-Tillers-Due-to-Injury-Hazard-Recall-Alert

Direct Canada link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2021/74615r-eng.php

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain John Deere’s Frontier-branded Rotary Tillers for use with Compact Utility Tractors.

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Otis Private Residence Elevator Recall [US]

Otis Private Residence Elevator Recall [US]

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US FlagUS/Washington: Otis Elevator Company, a Farmington, Connecticut establishment and CemcoLift Elevators Systems, formerly a Hatfield, Pennsylvania establishment, recall an estimated 5,000 Private Residence Elevators from the American marketplace due to suspected entrapment hazard with consequential risks of serious injury or death to young children, all serious safety hazards requiring immediate medical attention.

CPSC: http://ht.ly/aGUq30rrHH1

Direct link: https://www.cpsc.gov/Recalls/2021/Otis-Elevator-Company-Recalls-to-Inspect-Private-Residence-Elevators-Due-to-Entrapment-Hazard-Risk-of-Serious-Injury-or-Death-to-Young-Children

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain Otis Private Residence Elevators purchased before 2012 and CemcoLift Private Residence Elevators purchased from 1999 to 2012, as follows:

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Can-Am Off-Road Screw Jack Recall [US & Canada]

Can-Am Off-Road Screw Jack Recall [US & Canada]

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US FlagCanada FlagUS/Washington & Canada/Ottawa: BRP US Inc., a Sturtevant, Wisconsin establishment and Bombardier Recreational Products Inc., a Valcourt, Quebec establishment recall an estimated total 704 Can-Am branded Off-Road Screw Jacks (approximately 650 in the US and approximately 54 in Canada) from the American and Canadian marketplaces due to suspected structural collapse under load and consequential risks of falls, laceration, crush, concussion, bone fractures and/or central nervous system (“CNS”) injury, all serious health and safety hazards.

CPSC: http://ht.ly/Ky8830rrCe9; HCSC: http://ht.ly/BVFG30rrCe6

Direct US link: https://www.cpsc.gov/Recalls/2021/BRP-Recalls-Can-Am-Screw-Jacks-Due-to-Crush-Hazard

Direct Canada link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/74589r-eng.php

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain Can-Am Off-Road Screw Jacks sold as an accessory for Maverick X3 Side-By-Side Vehicles.

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Soho Fresh 70% Rubbing Alcohol Recall [US]

US FlagUS/Silver Spring: Soho Fresh 70% Rubbing Alcohol Recall [US]Essaar Inc., a Hackensack, New Jersey establishment, recalls certain batch/lots of Soho Fresh 70% Rubbing Alcohol from the American marketplace due to possible Methanol contamination (also called Methyl Alcohol or “Wood Alcohol”) from the American marketplace due to risks of poisoning, oral injury, internal ingestion, GI tract laceration damage, blindness and death, all serious health and safety hazards requiring immediate medical intervention.

FDA: http://ht.ly/QyQ530rrpb0

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/essaar-inc-issues-voluntary-nationwide-recall-rubbing-alcohol-contaminated-methanol

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Hand Sanitizer products are subject to this recall:

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Breakthrough Military-Grade Solvent Recall [Canada]

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Breakthrough Military-Grade Solvent Recall [Canada]

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Canada/Ottawa: Blue Line Solutions, a Vancouver, British Columbia establishment, recalls an estimated 3,574 Breakthrough Military-Grade branded Solvent products from the Canadian marketplace due to reported lack of child-resistant packaging and hazard information with consequential risks of oral injury, internal ingestion, GI tract laceration damage, bowel obstruction, developmental delays and/or long-term damage, reproductive delays, long-term damage, genetoxicity and/or mutagenicity, all serious health and safety hazards.

HCSC: http://ht.ly/tgha30rqZxC

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/74539r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports this recall involves certain batch/lots of Breakthrough Military-Grade Solvent, a liquid cleaner and degreaser, sold in spray containers of various sizes:

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US NHTSA Recalls: Volvo S60 & S80 Vehicles

US FlagWashington, DC: NHTSA Logo ColorAs of Monday, November 9, 2020, the US National Highway Traffic Safety Administration (“NHTSA”), a division of the US Department of Transportation, has posted a total of twenty-six (26) 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:
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MG Chemicals Epoxy Glue Recall [Canada]

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MG Chemicals Epoxy Glue Recall [Canada]

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Canada/Ottawa: MG Chemicals Ltd. a Burlington, Ontario establishment, recalls an estimated total 5013 units of MG Chemicals branded Epoxy Glue Products (an estimated 928 units of the Epoxy Kits and an estimated 4085 units of the Epoxy Dual Syringes) from the Canadian marketplace due to suspected failure to meet Canadian labelling and child-resistant packaging requirements for Quick Skin-Bonding Adhesives required by Canada’s Consumer Chemicals and Containers Regulations, 2001 under the Canada Consumer Product Safety Act and consequential risks of poisoning, oral injury, internal ingestion, GI tract laceration damage and death, all serious health and safety hazards.

HCSC: http://ht.ly/UHUI30rh5pn

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2020/74143r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports this recall involves six (6) MG Chemicals Epoxy Glue Products, five (5) Epoxy Kits and one (1) Dual Syringe.

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Barbie, Hot Wheels & PAW Patrol Hand Sanitizer Recall [US]

Barbie, Hot Wheels & PAW Patrol Hand Sanitizer Recall [US]

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US FlagUS/Silver Spring: Ashtel Studios, an Ontario, California establishment, recalls certain batch/lots of Children’s Character Licensed Hand Sanitizer products from the American marketplace due to reported resemblance to Children’s Food or Drink Containers and consequential risks of child poisoning, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/cG2y30rd7KO

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ashtel-studios-issues-voluntary-recall-licensed-hand-sanitizers-packaged-084-fluid-ounce-pouches-due

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Hand Sanitizer products are subject to this recall:

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DMM VISSION Cleaner Hand Sanitizer Recall [US]

Cleaner branded Hand Sanitizer Recall [US]

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US FlagUS/Silver Spring: DMM VISSION SA de CV, an Estado de México, México establishment, recalls at least five (5) batch/lots of Cleaner branded Hand Sanitizer from the American marketplace due to possible Methanol contamination (also called Methyl Alcohol or “Wood Alcohol”) from the American marketplace due to risks of poisoning, oral injury, internal ingestion, GI tract laceration damage, blindness and death, all serious health and safety hazards requiring immediate medical intervention.

FDA: http://ht.ly/XsbW30rcQ9x

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/dmm-vission-sa-de-cv-issues-voluntary-nationwide-recall-cleaner-hand-sanitizer-500-ml-and-1200-ml

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Hand Sanitizer products are subject to this recall:

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M branded Hand Sanitizer Alcohol Antiseptic Recall [US]

M branded Hand Sanitizer Alcohol Antiseptic 80%

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US FlagUS/Silver Spring: Medek, LLC, an Alamo, Texas establishment, recalls all current batch/lots of M branded Hand Sanitizer Alcohol Antiseptic 80% from the American marketplace due to possible Methanol contamination (also called Methyl Alcohol or “Wood Alcohol”) from the American marketplace due to risks of poisoning, oral injury, internal ingestion, GI tract laceration damage, blindness and death, all serious health and safety hazards requiring immediate medical intervention.

FDA: http://ht.ly/cBfc30raJ7f

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/medek-llc-issues-voluntary-nationwide-recall-m-hand-sanitizer-due-potential-presence-methanol-wood

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Hand Sanitizer products are subject to this recall:

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Fitting Furniture Bunk Bed Recall [Australia]

Fitting Furniture Bunk Bed Recall [Australia]

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Australia FlagAustralia/Canberra: Fitting Furniture, a Braeside, Victoria establishment, recalls certain batch/lots of Bunk Beds from the Australian marketplace due to suspected component failure and risks of structural failure, collapse, bone fracture, concussion, laceration and death, all serious safety hazards.

ACCC: http://ht.ly/G8oc30r91hW

Direct link: https://www.productsafety.gov.au/recall/fitting-furniture-various-bunk-beds

Additional information:
The Australian Competition & Consumer Commission (“ACCC”) reports the following Bunk Bed products are subject to this recall:

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BD Alaris Infusion Pump System Recall [US]

BD Alaris Infusion Pump System Recall [US]

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US FlagUS/Silver Spring: Becton, Dickinson and Company (“BDC”), a Franklin Lakes, New Jersey establishment, updates its existing recall for various models of BD Alaris Infusion Pump Systems from the American marketplace after an upgrading and reclassification of the original notification published by the US Food and Drug Administration (“FDA”) to Class I, the most serious and potentially deadly classification of medical device recall.

The original recall was initiated due to possible operational failure and consequential inaccurate dosage, failure to dose and possible life-changing complications including death, all serious health and safety hazards.

FDA: http://ht.ly/Irmt30r8C9r

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bd-provides-update-previously-disclosed-recall-bd-alaris-system-hardware

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Infusion Pump Systems are subject to this recall:

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Leafree Instant Hand Sanitizer Recall [US]

Leafree Instant Hand Sanitizer Recall [US]

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US FlagUS/Silver Spring: CorgioMed, LLC, a Gaithersburg, Maryland establishment, recalls all current batch/lots of Leafree Instant Hand Sanitizer-Aloe Vera from the American marketplace due to reported labelling as “EDIBLE ALCOHOL” and consequential risks of inadvertent alcohol poisoning, alcohol toxicity and GI tract laceration damage, all serious health and safety hazards.

FDA: http://ht.ly/466S30r8mCQ

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/corgiomed-llc-issues-voluntary-nationwide-recall-all-lots-leafree-instant-hand-sanitizer-aloe-vera

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Leafree Instant Hand Sanitizer products are subject to this recall:

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