WECK AutoEndo5 surgical clip appliers with model numbers listed may jam or misload, causing clips to fall out or break. Affected units include specific codes like 73J1600836. Contact WECK for details.
Certain clip appliers have an increase in misloading and/or jamming related complaints that may be due to a discrepancy in the specification a component. Misloading and/or jamming may lead to clips falling out of the applier, clip breakage, or the jaws becoming locked in a partially closed position (jammed).
WECK AutoEndo5 surgical clip appliers (model numbers listed in the record) may jam or misload, causing clips to fall out or break. This could lead to improper surgical procedures if used without the device functioning correctly.
The clip appliers have a discrepancy in a component specification that can cause misloading or jamming. This may result in clips falling out of the applier, clip breakage, or the jaws becoming locked in a partially closed position (jammed).
Surgical professionals who use these clip appliers during procedures are most at risk. Patients undergoing surgery with these devices could face complications if clips fail during the procedure.
Check for model numbers listed in the record, such as 73J1600836, 73C1700518, or 73D1800018. These devices were sold for surgical use and are identified by specific codes.
Look for the model number on the device, which is listed in the record (e.g., 73J1600836).
Reach out to WECK Medical for specific instructions on how to handle the device if it is affected.
The recall states that misloading or jamming may lead to clips falling out, breaking, or jaws jamming, which could affect surgical procedures. However, the record does not specify a risk of serious injury in normal use.
Check the model number on the device against the list of codes provided in the record, such as 73J1600836 or 73C1700518.
Contact WECK Medical for specific instructions on how to handle the device if it is affected.
We’ve drafted a message you can send WECK to request your refund or repair — edit it as you like.
Subject: Recall Z-0496-2020 — WECK WECK Hello, I own a WECK that is covered by recall Z-0496-2020 from WECK. 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.
