Baxter Healthcare recalls GEM4183C Coupler Force: Potential rust on forceps may cause issues. Check product code and lot numbers for affected items.
Potential presence of rust on Coupler Forceps (GEM4183C).
Baxter Healthcare is recalling GEM4183C Coupler Forceps due to potential rust. This could cause problems during medical procedures. Affected items have specific product codes and lot numbers.
Rust on the forceps could potentially cause issues during medical procedures. This might lead to complications if the rust affects the device's function or safety.
Healthcare professionals using the GEM4183C Coupler Forceps in medical settings are most at risk. Patients using these devices may also be affected if the rust causes complications.
Check for product code 5193-06001-010, lot number SP18E129-1307852, and sub-lot number 90828 on the packaging. The UDI is 00844735002850.
Look for product code 5193-06001-010, lot number SP18E129-1307852, and sub-lot number 90828 on the packaging.
The recall states potential rust on the forceps, but the record does not specify serious injury risks or immediate danger.
Check for product code 5193-06001-010, lot number SP18E129-1307852, and sub-lot number 90828 on the packaging.
The recall record does not specify a remedy, so no action is required beyond checking product details.
We’ve drafted a message you can send Baxter Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0680-2019 — Baxter Healthcare Baxter Healthcare Hello, I own a Baxter Healthcare that is covered by recall Z-0680-2019 from Baxter Healthcare. 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.
