Medline recalls HOI LUMBAR REF DYNJ902823G sterile packs due to incomplete sterilization. Affected units have Lot 20AKA895 expiring May 2021. Consumers should check product labels for this specific lot number.
The sterile pack inside the Complete Delivery System (CDS) did not go through a complete sterilization cycle, therefore the sterility of these components cannot be guaranteed.
Medline is recalling a specific lumbar delivery system sterile pack because it wasn't fully sterilized during manufacturing. This means the pack might not be sterile, which could lead to infections during medical procedures. Affected units have a specific lot number and expiration date.
The sterile pack inside the Complete Delivery System (CDS) did not complete a full sterilization cycle during manufacturing. This means the pack might not be sterile, which could lead to infections if used during medical procedures.
Healthcare professionals using the Medline HOI LUMBAR REF DYNJ902823G sterile pack with Lot 20AKA895 expiration May 2021 are most at risk. Patients receiving procedures using this pack could potentially be exposed to infection.
Check for the product label with 'HOI LUMBAR REF DYNJ902823G' and Lot 20AKA895 expiration date May 2021. The GTIN number is 0110193489219180.
Look for the lot number 20AKA895 and expiration date May 2021 on the sterile pack.
The recall states the sterility cannot be guaranteed due to incomplete sterilization, so it is not safe for medical use.
Check the label for 'HOI LUMBAR REF DYNJ902823G' with Lot 20AKA895 expiring May 2021 and GTIN 0110193489219180.
The recall does not specify a remedy, so contact Medline directly for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1357-2020 — Medline Medline Hello, I own a Medline that is covered by recall Z-1357-2020 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.
