Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
FLEX. GRASP. FORCEPS 6.6FR WL 550MM Recalled by Richard Wolf GmbH Due to Potentially unable to open forceps jaws when the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Richard Wolf GmbH directly.
Affected Products
FLEX. GRASP. FORCEPS 6.6FR WL 550MM, Product Number 8736.685
Quantity: 280 units
Why Was This Recalled?
Potentially unable to open forceps jaws when the endoscope shaft is bent by about 90 degrees. If, in addition, the proximal forceps shaft is bent, the forceps can no longer be opened or restrictions begin even with a slight bending of the endoscope.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Richard Wolf GmbH
Richard Wolf GmbH has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report