Medline Foot Ankle Kit Recall: Shelf-Life Component Discrepancy
Medline recalls 30 Foot Ankle Convenience Kits (SKU DYNJ65395A) due to shelf-life discrepancy in a component. Affected kits have UDI/DI 10195327174156 (each) or 40195327174157 (case) and Lot 22GBW912. Return to Medline for replacement.
Lower-risk recall
Discrepancy in the shelf-life of a component
What happened, in plain English
Medline is recalling 30 Foot Ankle Convenience Kits because a component has a shelf-life discrepancy. This could lead to the kit becoming ineffective or unsafe over time. Consumers should stop using the kits and contact Medline for a replacement. Read more at govinfonow.com/recall/1764689-medline-industries-lp-recalls-medline-convenience-kit-labeled-as-foot.
Source Summary by GovInfoNow · govinfonow.com/recall/1764689-medline-industries-lp-recalls-medline-convenience-kit-labeled-as-foot · Published October 27, 2026 · Updated October 27, 2026 · FDA enforcement record: FDA #Z-0189-2027
Cite this page
“Medline Foot Ankle Kit Recall: Shelf-Life Component Discrepancy.” GovInfoNow, updated October 27, 2026. https://govinfonow.com/recall/1764689-medline-industries-lp-recalls-medline-convenience-kit-labeled-as-foot. Based on FDA recall #Z-0189-2027 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0189-2027%22&limit=1).
Why it’s dangerous
The shelf-life of a component in the kit is incorrect, which may cause the kit to become ineffective or unsafe after the intended shelf life. This could lead to improper medical treatment if the kit is used beyond its safe period.
Who’s affected
Healthcare professionals and patients using the Foot Ankle Convenience Kit for medical purposes. Those with the specific lot number 22GBW912 are most at risk.
How to tell if you have this one
Check for the Medline convenience kit labeled 'FOOT ANKLE' with SKU DYNJ65395A. Look for UDI/DI numbers 10195327174156 (each) or 40195327174157 (case) and Lot Number 22GBW912.
- Brand
Medline- Category
Medical device
What to do — step by step
Stop using it now
The recalled kits have a shelf-life discrepancy in a component that could become ineffective or unsafe over time.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide distribution in the state of NY.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 40 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-0189-2027 (September 11, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0189-2027 to see it in context.
- Plain-language summary written by qwen3:4b on October 27, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.