Medline Convenience Kits for Anesthesia, Minor Procedures, Myringotomy and Cataract Surgery
Convenience kits may have open seals in sterile pouch packaging, which can compromise sterility and lead to contamination or patient infection.
Moderate risk
Using it may cause temporary or medically reversible health problems. Serious harm is unlikely.
FDA Class II recall · How risk is rated
What happened
Medline Industries, LP, of Northfield, Illinois, recalled convenience kits including CATARACT PACK DYNJ59881A, MINOR PACK DYNJ58421A SPRINGHILL MINOR PACK DYNJ40734F, MYRINGOTOMY PACK-LF DYNJ59097A, and ANESTHESIA PAIN PK LEAGUE DYNJ67925A because the kits may exhibit open seals in sterile pouch packaging.
An open seal may compromise product sterility, and if not detected prior to use, the issue may lead to contamination of the sterile field or patient infection. The company began the recall on July 31, 2026, and the FDA added it to the Enforcement Report on September 16, 2026. The kits were distributed in Arkansas, Florida, North Carolina, Maryland, and Texas.
Summary by Recall Canary from the FDA notice.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is your kit affected?
4 products
Affected if its UDI-DI and lot code are listed under that product.
Convenience kits Cataract Pack DYNJ59881A
- UDI-DI
- 10198459020612
- Lot
- 25GBP246
Convenience Kits Minor Pack DYNJ58421A Springhill Minor Pack DYNJ40734F
- UDI-DI
- 10193489970487
- 10198459162084
- Lot
- 25HBQ049
- DYNJ40734F
- 25GBO299
- 25IBS607
Convenience kits Myringotomy Pack-LF DYNJ59097A
- UDI-DI
- 10198459046551
- Lot
- 25FBU754
Convenience kits Anesthesia Pain PK League DYNJ67925A
- UDI-DI
- 10195327506506
- Lot
- 25BBK494
Details
- Company began the recall
- Sold in
US Nationwide distribution in states of Arkansas, Florida, North Carolina, Maryland, and Texas.
- Event ID
- 99667
- Recall numbers
- Z-3207-2026 to Z-3210-2026
- Company
- Medline Industries, LPNorthfield, Illinois
- Hazard
- Sterility failure
- Recall type
- Voluntary: Firm initiated
- Customers told by
- Letter
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
