Weleda Baby Teething Powder Recall [Australia]

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Australia/Canberra: Weleda Australia Pty Ltd, a Warriewood, New South Wales establishment, recalls certain batch/lots of Weleda Baby Teething Powder due to suspected component detachment and plastic fragment contamination and consequential risk of choking, oral injury, internal ingestion and GI tract laceration damage, a serious health

ACCC: http://ht.ly/bGU030oFEgx

Direct link: https://www.productsafety.gov.au/recall/weleda-australia-pty-ltd-weleda-baby-teething-powder-60g

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

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ThermaCare Back Pain Therapy HeatWrap Recall [US]

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US/Silver Spring: Pfizer Consumer Healthcare, a division of Pfizer Inc., a New York, New York establishment, recalls certain batch/lots of ThermaCare Back Pain Therapy HeatWraps due to suspected failure to higher cell temperature than specified and consequential risk of skin injuries such as burns, blisters and/or skin irritation on the exposed skin.

FDA: http://ht.ly/e5KJ30oyKxG

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/pfizer-inc-issues-voluntary-nationwide-consumer-level-recall-one-lot-thermacarer-back-pain-therapy

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

DG/Health Naturals Baby Cough Syrup Recall [US]

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US/Silver Spring: Kingston Pharma, LLC, a Massena, New York establishment, recalls certain batch/lots of DG/Health Naturals Baby Cough Syrup + Mucus due to suspected risk of Bacillus Cereus / Bacillus Circulans contamination and consequential risk of Gram-negative bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/bvsE30o7Z2E

Direct link: https://www.fda.gov/Safety/Recalls/ucm634052.htm

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

Tweed Dried Cannabis Recall [Canada]

Canada/Ottawa: Tweed, Inc., a Smiths Falls, Ontario establishment, recalls an estimated 13,575 units of LBS Sunset (Indica) Dried Cannabis due to suspected mislabeling and consequential incorrect Cannabinoid values with risks of overdose, all serious health and safety hazards.

HCSC: http://ht.ly/y8Zm30o3CFJ

Direct link: https://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/69256r-eng.php

Additional information:
Health Canada/Santé Canada (“HCSC”) reports this recall involves one (1) batch/lot consisting of Tweed branded LBS Sunset (Indica) Dried Cannabis sold through authorized provincial and territorial retailers in British Columbia, Alberta, Saskatchewan, Manitoba, Ontario, Quebec, New Brunswick, Nova Scotia, Newfoundland, Prince Edward Island, Northwest Territories and Nunavut, as follows:

EZY Gel Topical Anesthetic Gel Recall [US]

US/Washington: Biotouch Inc., a City of Industry, California recalls an estimated 8,500 EZY Gel Topical Anesthetic Gel due to suspected failure to meet US Child Resistant Closure Requirement and consequential risk of poisoning, both serious health and safety hazards.

CPSC: http://ht.ly/NN8P30nYMRn

Direct link: https://www.cpsc.gov/Recalls/2019/Biotouch-Recalls-Topical-Anesthetic-Due-to-Failure-to-Meet-Child-Resistant-Closure-Requirement-Risk-of-Poisoning

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain containers of EZY Gel Topical Anesthetic Gel.

St John Ambulance First Aid Kit Recall [Australia]

Australia/Canberra: St John Ambulance Australia, a Burnwood, New South Wales establishment, recalls certain batch/lots of Tiny Tots First Aid Kits due to suspected component detachment and consequential risk of choking, oral injury, internal ingestion, burns and GI tract laceration damage, all serious health and safety hazards.

ACCC: http://ht.ly/z8BO30nEqgC

Direct link: https://www.productsafety.gov.au/recall/st-john-ambulance-australia-tiny-tots-first-aid-kit

Additional information:
The Australian Competition & Consumer Commission (“ACCC”) reports the following First Aid Kits are subject to this recall:

Stryker Lifepak 15 Monitor/Defibrillator Recall [US]

US/Silver Spring: Stryker, a Kalamazoo, Michigan establishment, recalls an estimated 13,003 Lifepak 15 Monitor/Defibrillator Medical Devices due to suspected operational malfunction and consequential risk of device lock-up after a defibrillation shock is delivered and subsequent failure to function, possibly leading to delay or complete failure of the device to operate in an emergency and possible injury and/or death, all serious health and safety hazards. Deaths reported.

FDA: http://ht.ly/1P0530nAsHs

Direct link: https://www.fda.gov/Safety/Recalls/ucm630455.htm

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Monitor/Defibrillator Medical Devices are subject to this recall: