Medline Industries, LP is recalling 54,301 medical convenience kits containing BD ChloraPrep Triple Swabsticks. These kits were distributed nationwide and include various sets for anesthesia, catheter dressing, dialysis, and surgical procedures. The recall was initiated because the swabstick applicators inside the kits may have open seals on their individual packaging, which can compromise the sterility of the medical device.
An open seal on the swabstick packaging could allow the sterile applicators to become contaminated. Using a non-sterile device during medical procedures increases the risk of serious infections for patients.
Recall #: Z-1326-2026; Quantity: 120 kits
Recall #: Z-1327-2026; Quantity: 1350 kits
Recall #: Z-1328-2026; Quantity: 450 kits
Part of Recall #: Z-1329-2026
Part of Recall #: Z-1329-2026
Part of Recall #: Z-1329-2026
Part of Recall #: Z-1329-2026
Part of Recall #: Z-1329-2026
Part of Recall #: Z-1329-2026
Part of Recall #: Z-1329-2026
Part of Recall #: Z-1330-2026
Part of Recall #: Z-1330-2026
Part of Recall #: Z-1330-2026
Part of Recall #: Z-1330-2026
Part of Recall #: Z-1330-2026
Part of Recall #: Z-1330-2026
Part of Recall #: Z-1330-2026
Part of Recall #: Z-1330-2026
Part of Recall #: Z-1330-2026
Part of Recall #: Z-1331-2026
Part of Recall #: Z-1331-2026
Recall #: Z-1332-2026
Recall #: Z-1333-2026
Part of Recall #: Z-1334-2026
Part of Recall #: Z-1334-2026
Part of Recall #: Z-1334-2026
Part of Recall #: Z-1334-2026
Part of Recall #: Z-1334-2026
Part of Recall #: Z-1334-2026
Part of Recall #: Z-1334-2026
Part of Recall #: Z-1334-2026
Part of Recall #: Z-1334-2026
Recall #: Z-1335-2026
Recall #: Z-1336-2026
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES ยท Raw API Response
openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.