Medline recalls specific arthroscopy packs due to plastic syringe leaks and breakage that could harm patients. Affected kits have unique pack numbers and lot codes. Consumers should check their kits for these identifiers.
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
Medline is recalling arthroscopy procedure kits that contain plastic syringes prone to leaks and breakage. This poses a risk to patient health during medical procedures, so affected users should stop using these kits immediately.
The plastic syringes in these kits can leak or break, potentially causing contamination or injury to patients during medical procedures. This risk is linked to FDA safety alerts about quality issues in the kits.
Healthcare professionals using the recalled Medline procedure kits are most at risk. Patients receiving procedures with these kits could be harmed by leaks or breakage.
Check for specific pack numbers: DYNJHS0101I, DYNJ0390808F, DYNJ23150J, DYNJ21233O, DYNJ46435A, or DYNJ50120D. Also look for lot numbers like 21LBA780A, 21JMG164A, and others listed in the recall notice.
If you have any of the recalled Medline arthroscopy procedure kits with the listed pack numbers and lot codes, stop using them right away to prevent potential harm.
The recall includes arthroscopy packs with pack numbers DYNJHS0101I, DYNJ0390808F, DYNJ23150J, DYNJ21233O, DYNJ46435A, and DYNJ50120D, each with specific lot numbers.
Check the pack number and lot number on your Medline procedure kit. Affected kits have the specific pack numbers and lot codes listed in the recall notice.
The recall record does not mention any remedy or replacement options. Affected users should stop using the kits immediately.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1452-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1452-2025 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.
