Richard Wolf recalls FLEX Biopsy Forceps 5FR WL 550MM with potential inability to open jaws when endoscope shaft bends 90 degrees. Affected units have specific lot numbers.
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 Biopsy Forceps 5FR WL 550MM because they might not open properly if the endoscope shaft bends. This could cause problems during medical procedures if the forceps can't be opened.
The forceps may not open when the endoscope shaft bends 90 degrees. If the proximal shaft also bends, the forceps can't be opened even with slight bending of the endoscope, potentially causing procedure failures.
Medical professionals using these forceps during endoscopic procedures are most at risk. Patients undergoing procedures with these forceps could face complications if the forceps malfunction.
Check for the product number 829.051 and lot numbers listed: 4500377840, 4500377840, 4500377840, 4500376297, 4500371970, 4500363663, 4500363098, 4500361404, 4500353562, 4500349168, 4500347747, 4500338560, 4500333999.
Verify the product number 829.051 and lot numbers listed in the recall notice.
The forceps may not open properly if the endoscope shaft bends 90 degrees, which could lead to procedure complications.
Check for product number 829.051 and lot numbers: 4500377840, 4500377840, 4500377840, 4500376297, 4500371970, 4500363663, 4500363098, 4500361404, 4500353562, 4500349168, 4500347747, 4500338560, 4500333999.
The recall notice does not specify a remedy, so contact Richard Wolf directly for guidance.
We’ve drafted a message you can send Richard Wolf to request your refund or repair — edit it as you like.
Subject: Recall Z-1423-2023 — Richard Wolf Richard Wolf Hello, I own a Richard Wolf that is covered by recall Z-1423-2023 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.
