Richard Wolf recalls FLEX GRASP FORCEPS 5FR WL 550MM (Product #828.051) due to potential inability to open forceps 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 GRASP 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 become stuck.
The forceps may not open if the endoscope shaft bends about 90 degrees. If the proximal shaft also bends, the forceps can't open even with minor bending of the endoscope, potentially causing procedure issues.
Medical professionals using the FLEX GRASP FORCEPS 5FR WL 550MM during endoscopic procedures. Those with specific lot numbers from the list are most at risk.
Check for Product Number 828.051 and specific lot numbers listed in the recall notice. The units were sold with UDI/DI: 04055207009574.
Verify your FLEX GRASP FORCEPS 5FR WL 550MM has Product Number 828.051 and one of the listed lot numbers.
The forceps may not open properly if the endoscope shaft bends 90 degrees, which could cause issues during medical procedures.
The recall notice does not specify a remedy; check if your unit has the Product Number 828.051 and a listed lot number.
Look for Product Number 828.051 and one of the specific lot numbers listed in the recall notice.
We’ve drafted a message you can send Richard Wolf to request your refund or repair — edit it as you like.
Subject: Recall Z-1422-2023 — Richard Wolf Richard Wolf Hello, I own a Richard Wolf that is covered by recall Z-1422-2023 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.
