Reported Apr 29, 2026 · Ongoing
Medline Kits: 1) D AND C PACK, Model Number: DYNJ41254B
Medline Industries, LP
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medline Industries, LP · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
- Medline Kits1) D AND C PACK
- Model NumberDYNJ41254B
- Lot codes and dates
- 1) DYNJ41254B
- UDI-DI
10888277882003(each)40888277882004(case)
- Lot Number25FBA224
- Amount recalled
- 12 units
This recall covers 39 products
The agency filed one notice per product. You are reading one of them; the other 38 are below.
26 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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