Medline recalls sterile needle counters with potential packaging seal issues that could compromise sterility. Affected lots include 67016114501-67017104502. Consumers should check their product lot numbers.
The product packaging seal has the potential to experience seal creep. This may result in gaps to be created in the seals of the packaging and may impact the sterility of the Needle Counters.
Medline is recalling sterile needle counters that may have packaging seals that could develop gaps, potentially compromising sterility. This could lead to contamination during surgical procedures if the needles are not properly sterile.
The packaging seal may experience 'seal creep,' creating gaps that could allow contamination. This might compromise the sterility of the needle counters, which are used to track surgical sharps during procedures.
Surgical staff and hospitals using Medline sterile needle counters with the specified lot numbers are most at risk. The product is designed for surgical use but does not contact patients directly.
Check your Medline sterile needle counter lot numbers: 67016114501 through 67017104502. The product is a 40-count foam block with adhesive, used for surgical sharps counting.
Identify your Medline sterile needle counter's lot number from the packaging. Affected lots are 67016114501 through 67017104502.
The packaging seal may experience 'seal creep,' potentially creating gaps that could compromise sterility of the needle counters.
Check your lot number. If it's in the affected range (67016114501-67017104502), stop using it and contact Medline for instructions.
The product is safe for use if the packaging seal remains intact. However, the recall indicates a potential risk of compromised sterility if the seal develops gaps.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1932-2018 — Medline Medline Hello, I own a Medline that is covered by recall Z-1932-2018 from Medline. 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.
