Medline Sterile Procedural Trays Risk Puncture from Blades

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Contact the company & request your remedy

Recalling firmMEDLINE INDUSTRIES, LP - Northfield3 Lakes Dr · Northfield, IL 60093-2753

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Medline is recalling sterile procedural trays labeled 'DR MOTT DRA:PE PACK' because sterile blades inside the trays could puncture the outer foil packaging. This risk could lead to contamination of the trays during medical procedures.

Why it’s dangerous

Sterile blades inside the trays can puncture the outer foil layer of the packaging. This could allow contaminants to enter the sterile trays, potentially causing infections during medical procedures.

Who’s affected

Healthcare professionals using these trays for medical procedures are most at risk. Patients and staff could be exposed to contamination if the packaging is punctured.

How to tell if you have this one

Check for trays labeled 'DR MOTT DRAPE PACK'. Look for item number DYNJ42065B, case UDI/GTIN 40888277893550, and unit UDI/GTIN 10888277893559. Lot number 22JLA859 is also associated with these units.

Brand
Medline Industries
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Label
Look for the label 'DR MOTT DRAPE PACK' on the tray.
Verify Item Details
Confirm the item number DYNJ42065B, case UDI/GTIN 40888277893550, and unit UDI/GTIN 10888277893559.

✎ GovInfoNow

Questions people ask

Why is this recall happening?

Sterile blades inside the trays could puncture the outer foil packaging, risking contamination during medical procedures.

What should I do if I have this product?

Check the product label for 'DR MOTT DRAPE PACK' and verify the item details. If affected, contact Medline for guidance.

Is there a deadline to act?

The recall notice does not specify a deadline for action.

Take action

Contact Medline Industries

We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1086-2023 — Medline Industries Medline Industries

Hello,

I own a Medline Industries that is covered by recall Z-1086-2023 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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Where this comes from

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.

Official source: FDA Recall #Z-1086-2023 (November 17, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1086-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

MEDLINE INDUSTRIES, LP - Northfield recalls Sterile Procedural Trays, labeled as the following: DR MOTT DRAPE PACK

Lower-risk recall