Family Dollar Cosmetics, Foods, Drugs & Supplements [US]

US FlagUS/Silver Spring: Logo - Family DollarFamily Dollar, a Charlotte, North Carolina establishment, recalls all current batch/lots of numerous Cosmetics, Dietary Supplements; Drugs, Medical Devices, as well as Human and Pet Foods sold by 404 Family Dollar stores that received products from Family Dollar Distribution Center number 202 located in West Memphis, Arkansas, due to rodent infestation and the potential presence of Salmonella with consequential risks of Gram-negative bacterial infection, severe illness and/or possible life-changing complications, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

FDA: http://ht.ly/LzXX30sbsG3

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/family-dollar-stores-issues-voluntary-recall-certain-fda-regulated-products-six-states-including

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

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TTDeye Contact Lens Recall [US]

TTDeye Contact Lens Recall [US]

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US FlagUS/Silver Spring: Chengdu Ai Qin E-commerce Co., Ltd. recalls an estimated 1362 pairs of TTDeye branded Colored Contact Lenses from the American marketplace due to suspected failure to gain FDA mandatory pre-sale safety approvals and risk of eye damage and/or blindness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/IOr530qUB5Y

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/chengdu-ai-qin-e-commerce-co-ltd-issues-nationwide-recall-ttdeye-brand-colored-contact-lenses

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

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Biocell Breast Implant & Tissue Expander Recall [US]

US FlagUS/Silver Spring: Logo - Allergan AestheticsAllergan Aesthetics, an Irvine, California establishment and subsidiary of AbbVie of North Chicago, Illinois, recalls an estimated 52,000 Biocell Breast Implants and/or Tissue Expanders from the American marketplace due to suspected risk of Breast Implant Associated Anaplastic Large Cell Lymphoma (“BIA-ALCL”), a type of Non-Hodgkin’s Lymphoma (Cancer of the Immune System) and consequential risk of possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/j7Bw30qN5k9

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/allergan-aesthetics-launches-dedicated-multi-channel-campaign-contact-patients-who-may-not-be-aware

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Breast Implants and/or Tissue Expanders are subject to this recall:

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Hollister Urostomy Bag Recall [Australia]

Australia FlagAustralia/Canberra: Logo - Liberty Medical PtyLiberty Medical Pty Ltd, a Box Hill, Victoria establishment, recalls certain batch/lots of Hollister branded Urostomy Bags due to suspected film failure and consequential risk of local site injury and bacterial infection, all serious health and safety hazards.

ACCC: http://ht.ly/nefX30plhUo

Direct link: https://www.productsafety.gov.au/recall/liberty-medical-pty-ltd-hollister-urostomy-bag

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

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Stryker Lifepak 15 Monitor/Defibrillator Recall [US]

US FlagUS/Silver Spring: Stryker Lifepak 15 Monitor/Defibrillator Recall [US]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:

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