Richard Wolf recalls FLEX GRASP FORCEPS 5FR WL 550MM with potential inability to open jaws when endoscope shaft bends 90 degrees. Affected units have specific lot numbers and product codes.
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.
Richard Wolf is recalling FLEX GRASP FORCEPS 5FR WL 550MM surgical instruments because they may not open properly if the endoscope shaft bends. This could lead to complications during medical procedures if the forceps become stuck.
If the endoscope shaft bends about 90 degrees, the forceps jaws may not open. If the proximal shaft also bends, the forceps can't open even with slight bending of the endoscope, potentially causing procedure complications.
Surgical professionals using these forceps during procedures are most at risk. Patients and medical staff who have the specific lot numbers listed in the recall are affected.
Check for the product number 8735.685 and lot numbers listed in the recall (e.g., 4500377618, 4500377296). These forceps are sold for medical use in the U.S. by Richard Wolf GmbH.
Look for the product number 8735.685 and lot numbers listed in the recall (e.g., 4500377618, 4500377296) on the instrument packaging or label.
The forceps may not open properly if the endoscope shaft bends 90 degrees, which could lead to procedure complications if the proximal shaft also bends.
Check for the product number 8735.685 and lot numbers listed in the recall (e.g., 4500377618, 4500377296) on the instrument packaging or label.
The recall does not specify a remedy, so contact Richard Wolf directly for guidance on next steps.
We’ve drafted a message you can send Richard Wolf to request your refund or repair — edit it as you like.
Subject: Recall Z-1424-2023 — Richard Wolf Richard Wolf Hello, I own a Richard Wolf that is covered by recall Z-1424-2023 from Richard Wolf. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
