Centurion Medical recalls surgery convenience kits with incomplete sterile package seals that may compromise sterility. Affected kits include subclavian on/off kits, SDS procedure packs, and biopsy packs from specific lot numbers. Consumers should contact the company for details.
Incomplete seals on the sterile package may compromise the sterility
Centurion Medical recalls several surgery convenience kits because their sterile packaging may have incomplete seals, risking infection during procedures. This is a serious safety issue for medical professionals using these kits in surgeries.
The sterile packaging for these kits may have incomplete seals, which can allow contamination. This could lead to infections during surgical procedures if the kits are not properly sterile.
Medical professionals who use these kits during surgery are most at risk. Patients undergoing procedures with these kits could face infection if the sterility is compromised.
Check for the product names: Subclavian On/Off Kit (DYNDH1033B), SDS Procedure Pack (DYNDH1090A), and Biopsy Packs (DYNDH1110, DYNDH1114). Look for specific lot numbers listed in the recall notice.
Identify the product name and lot number from the recall list to confirm if your kit is affected.
Reach out to Centurion Medical Products Corporation for further instructions on handling affected kits.
The recall states that incomplete seals may compromise sterility, so affected kits should not be used until the manufacturer provides instructions.
Contact Centurion Medical Products Corporation directly for specific guidance on handling the affected kits.
Check the product name and lot number against the list provided in the recall notice.
We’ve drafted a message you can send Centurion to request your refund or repair — edit it as you like.
Subject: Recall Z-1052-2020 — Centurion Centurion Hello, I own a Centurion that is covered by recall Z-1052-2020 from Centurion. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
