Medline recalls sterile procedural trays that may have blades puncturing packaging foil. Affected items include specific eye and vitreous packs with lot numbers from 22JDA005 to 22JBW843. No remedy is listed.
Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
Medline is recalling sterile procedural trays that could have blades puncturing the outer foil packaging. This risk might lead to contamination during medical procedures if the packaging is compromised.
Sterile blades inside the trays might puncture the foil layer of the packaging during use. This could allow contamination to reach the surgical site, potentially causing infections.
Healthcare professionals using these trays for eye surgeries or procedures are most at risk. Patients receiving these trays could be exposed to contamination if the packaging is punctured.
Check for specific product names like BASIC EYE PACK-LF, VITRECTOMY PACK-LF, or EYE PACK-EAST-LF. Look for lot numbers starting with 22JDA005 through 22JBW843 on the packaging.
Look for the product names and lot numbers listed in the recall notice to confirm if your item is affected.
The recall is due to the potential for sterile blades to puncture the outer foil packaging, which could lead to contamination during medical procedures.
The recall notice does not specify a remedy, so you should check the product labels for the affected lot numbers and contact Medline if you are unsure.
Yes, lot numbers from 22JDA005 to 22JBW843 are affected. Check your product's lot number to see if it falls within this range.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-1095-2023 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-1095-2023 from Medline 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.
