CooperSurgical recalls Silver-Plated Copper Sims Uterine Sound (Part 64-6: 00888937017762) due to incorrect part number laser marking during manufacturing. This may cause confusion in identifying the correct device.
During the manufacturing process the devices were laser-marked with the incorrect part number.
CooperSurgical is recalling Silver-Plated Copper Sims Uterine Sounds with part number 64-600 because they were laser-marked with the wrong part number during production. This could lead to confusion about which device is being used, potentially causing errors in medical procedures.
The devices were laser-marked with the incorrect part number during manufacturing. This could cause confusion when identifying the correct device, potentially leading to errors in medical procedures if the wrong device is used.
Healthcare providers who use this specific uterine sound during medical procedures may be affected. Patients using the device are at low risk if the incorrect marking doesn't impact the device's function.
Check for the part number 64-600 on the device. The unique device identifier (UDI-DI) is 00888937017762. This product was sold by CooperSurgical.
Look for the part number 64-600 and unique device identifier (UDI-DI) 00888937017762 on the device.
The devices were laser-marked with the incorrect part number during manufacturing, which could cause confusion in identifying the correct device.
Check the device label for part number 64-600 and UDI-DI 00888937017762. If you have this specific model, you may need to contact CooperSurgical for further instructions.
The recall is due to a labeling issue, not a safety hazard. There is no risk of injury from the device itself.
We’ve drafted a message you can send CooperSurgical to request your refund or repair — edit it as you like.
Subject: Recall Z-3188-2024 — CooperSurgical CooperSurgical Hello, I own a CooperSurgical that is covered by recall Z-3188-2024 from CooperSurgical. 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.
