Convenience kits recallZ-3207-2026 · Medline Industries, LP · initiated Jul 31, 2026
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Medline Industries, LP or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
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.
FDA root cause category: Under Investigation by firm
What the company is doing
Firm began notifying customers on July 31, 2026 via email and first-class mail. Customers were instructed to discard any affected sterile convenience kits.
Recall details
- Recall number
- Z-3207-2026
- Status
- Open, Classified
- Initiated by the company
- Jul 31, 2026
- Posted by the FDA
- Sep 16, 2026
- Recalling firm
- Medline Industries, LP
- Quantity
- 341
- Product code
- OFT
- Distribution
- US Nationwide distribution in states of Arkansas, Florida, North Carolina, Maryland, and Texas.
Product description
Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A
Code information (models, lots, serial numbers)
UDI-DI 10195327506506 Lot 25BBK494
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- Medline Industries, Inc. DYNJ67925AMedline Industries, Inc. · Spinal epidural anesthesia kit1 recall1 report
Other products in the same recall event
The FDA groups related products into one recall event (event 99667).
- Z-3208-2026 · Open, ClassifiedConvenience kits MINOR PACK DYNJ58421A SPRINGHILL MINOR PACK DYNJ40734F
- Z-3209-2026 · Open, ClassifiedConvenience kits MYRINGOTOMY PACK-LF DYNJ59097A
- Z-3210-2026 · Open, ClassifiedConvenience kits CATARACT PACK DYNJ59881A
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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