International Medical Industries recalls Prep-Fill Guarded Luer Connectors with unsealed blister packaging that could compromise sterility during medical use.
Blister package had an unsealed edge compromising sterility.
International Medical Industries is recalling Prep-Fill Guarded Luer Connectors due to blister packages with unsealed edges that might compromise sterility. This could lead to infections if the connectors are used in medical procedures without proper sterility.
The blister package had an unsealed edge, which could allow contamination and compromise sterility. This risk is specific to medical use where sterility is critical for preventing infections.
Healthcare professionals and medical facilities using the Prep-Fill Guarded Luer Connectors with specific part numbers and lot numbers listed in the recall notice.
Check for part numbers 57-400, 57-400W, 57-401, 57-402, or 57-403 with specific lot numbers listed in the recall notice. The unique device identifier (UDI) codes are also provided for identification.
Identify the part number and lot numbers listed in the recall notice to determine if your connector is affected.
The blister package had an unsealed edge that could compromise sterility during medical procedures.
Prep-Fill Guarded Luer Connectors with part numbers 57-400, 57-400W, 57-401, 57-402, or 57-403 and specific lot numbers listed in the recall notice.
The recall does not require immediate stop use; affected products should be checked against the listed part numbers and lot numbers.
We’ve drafted a message you can send International Medical Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-0925-2023 — International Medical Industries International Medical Industries Hello, I own a International Medical Industries that is covered by recall Z-0925-2023 from International Medical Industries. 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.
