Reported Jan 22, 2025 · Ongoing
Medical procedure kits labeled as
Sklar Instruments
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: Sklar Instruments · 1333 Lenape Rd · West Chester, PA · 19382-6816
Is this the product you have?
Medical procedure kits labeled as
4 of 4 products
| Model / number | Product as published |
|---|---|
96-2540 | ECONO STERILE STRABIS SCISS STR 4.5"STER 50 |
96-2541 | ECONO STERILE STRABIS SCISS CVD 4.5"STER 50 |
96-2542 | ECONO STERILE STRABIS SCISS STR 4.5"STER 25 |
96-2542M | ECONO STERILE STRABISMUS SCISS STR4.5"CS/25, ; eye surgery |
- Lot codes and dates
1) 96-2540UDI/DI 50649111054967
- Lot codes
FSS8FSS102) 96-2541UDI/DI 50649111055087
- Lot codes
FSS103) 96-2542UDI/DI 50649111055391
- Lot codes
FSS104) 96-2542MUDI/DI 50649111440685
- Lot codesMSS10
- Amount recalled
- 350 units
This recall covers 30 products
The agency filed one notice per product. You are reading one of them; the other 29 are below.
17 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Reports of various packaging issues that may result in a breach of the sterile barrier.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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