Richard Wolf recalls FLEX GRASP FORCEPS 6.6FR WL 550MM (Product #8736.685) due to potential inability to open forceps jaws when endoscope shaft bends 90 degrees, risking medical procedures.
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 6.6FR WL 550MM models because they might not open properly if the endoscope shaft bends. This could cause problems 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 minor bending of the endoscope, potentially causing procedure delays or errors.
Medical professionals using the FLEX GRASP FORCEPS 6.6FR WL 550MM during procedures are most at risk if the endoscope shaft bends. Patients using these tools could face complications if the forceps malfunction.
Check for Product Number 8736.685 on the device. The lot numbers listed (e.g., 4500377853) are part of the affected batch. These forceps were sold with specific UDI/DI codes.
Look for Product Number 8736.685 on the device to confirm if it's affected.
Reach out to Richard Wolf GmbH for specific guidance on handling the device if it's affected.
The forceps may not open properly if the endoscope shaft bends 90 degrees, which could cause procedure issues.
Check for Product Number 8736.685 and the listed lot numbers (e.g., 4500377853) on the device.
Contact Richard Wolf GmbH for specific instructions on handling the device if it's affected.
We’ve drafted a message you can send Richard Wolf to request your refund or repair — edit it as you like.
Subject: Recall Z-1425-2023 — Richard Wolf Richard Wolf Hello, I own a Richard Wolf that is covered by recall Z-1425-2023 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.
