Reported Mar 19, 2025 · Ongoing
Numerous models of nonsterile hemostatic forceps
Aesculap Inc.
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: Aesculap Inc · 3773 Corporate Pkwy · Center Valley, PA · 18034-8217
Is this the product you have?
Numerous models of nonsterile hemostatic forceps
13 of 13 products
| Model / number | Product as published |
|---|---|
FB458R | (1) , Glover ATR.CLAMP CVD 215MM |
FB459R | (2) , Glover ATR.CLAMP CVD 245MM |
FB461R | (3) , Glover ATR.CLAMP 195MM |
FB462R | (4) , Glover ATR.CLAMP 210MM |
FB469R | (5) , Leland-Jones Peripheral CLMPSTR 195MM |
FB567R | (6) , Cooley Pediatric Clamp 30DG30/165MM |
FB568R | (7) , Cooley Pediatric Clamp 60DG 30/160MM |
FB569R | (8) , Cooley Pediatric Clamp 90DG30/150MM |
FB729R | (9) , Cooley Pediatric Clamp 17MM 170MM |
FB730R | (10) , Cooley Pediatric Clamp 20MM175MM |
FB736R | (11) , Cooley Pediatric Clamp 74MM 185MM |
FB737R | (12) , Cooley Pediatric Clamp 86MM 195MM |
FB738R | and (13) , Cooley Pediatric Clamp 108MM 260MM. |
- Amount recalled
- 1,147 forceps
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
- Nationwide
- PR
Why it was recalled
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
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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