Medline Industries, LP recalls Convenience kits MYRINGOTOMY PACK-LF DYNJ59097A
- Recalling company
- Medline Industries, LP
- Product
- Convenience kits MYRINGOTOMY PACK-LF DYNJ59097A
- Reason
- Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Jul 31, 2026
- Reported
- Sep 23, 2026
- Distribution
- US Nationwide distribution in states of Arkansas, Florida, North Carolina, Maryland, and Texas.
- Status
- Ongoing
- Quantity
- 60
- Lot / codes
- UDI-DI 10198459046551 Lot 25FBU754
- Company location
- Northfield, IL
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-3209-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-3209-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.