Medline recalls procedural kits with plastic syringes that may leak or break, posing health risks. Affected kits include BOTOX KIT - CHRONIC MIGRAINE and BREAST packs with specific pack and lot numbers.
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 procedural kits that contain plastic syringes with potential leaks or breakage, which could harm patients. These kits include specific BOTOX and BREAST products with listed pack and lot numbers. The recall addresses safety concerns from FDA alerts about quality issues in the syringes.
The plastic syringes in these kits may leak or break, which could lead to patient health risks. This issue was identified through FDA safety alerts from March 2024, indicating potential quality problems with the syringes.
Healthcare providers and patients using the recalled procedural kits, particularly those with the specific BOTOX KIT - CHRONIC MIGRAINE and BREAST packs listed by pack number and lot number.
Check for kits labeled as BOTOX KIT - CHRONIC MIGRAINE (Pack Number DYKM2000) or BREAST (Pack Number DYNJ902703K) with specific lot numbers listed in the recall.
Look for the specific pack numbers and lot numbers listed in the recall to identify affected kits.
The recall includes Medline procedural kits labeled as BOTOX KIT - CHRONIC MIGRAINE (Pack Number DYKM2000) and BREAST (Pack Number DYNJ902703K), among others with specific pack and lot numbers.
The recall is due to plastic syringes in these kits potentially leaking or breaking, which could pose health risks as identified by FDA safety alerts from March 2024.
No immediate stop is required; the recall addresses a low-risk hazard where the kits may leak or break, but the remedy is to check labels and avoid use if affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2750-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2750-2024 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.
