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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