CLASS II ONGOING Device recall · Reported 2 Oct 2024 · FDA Enforcement Report

Silver-Plated Copper Sims Uterine Sound recalled by CooperSurgical

CooperSurgical is recalling Silver-Plated Copper Sims Uterine Sound, distributed nationwide in the US. The recall was initiated on 31 Jul 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesUDI-DI: 00888937017762; Part Numbers: 64-600
Quantity recalled468 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-3188-2024
FDA event ID
95232
Recalling firm
CooperSurgical, Trumbull, CT
Classification
Class II
Status
Ongoing
Recall initiated
31 Jul 2024
FDA classified
20 Sep 2024
Reported
2 Oct 2024
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons

Timeline

31 Jul 2024Recall initiated by company
20 Sep 2024Classified by FDA+51 days
2 Oct 2024Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

During the manufacturing process the devices were laser-marked with the incorrect part number.

Product as listed by the FDA

Silver-Plated Copper Sims Uterine Sound, Part Number 64-600

Where it was distributed

Worldwide distribution - US Nationwide and the countries of Armenia, Bahrain, Canada, Hong Kong, India, New Zealand, Qatar, Sweden.

Nationwide

Questions about this recall

Is Silver-Plated Copper Sims Uterine Sound recalled?

Yes. CooperSurgical recalled Silver-Plated Copper Sims Uterine Sound on 31 Jul 2024. The recall is Class II and its status is Ongoing. Recall number Z-3188-2024.

Why was it recalled?

During the manufacturing process the devices were laser-marked with the incorrect part number.

Which lots are affected?

UDI-DI: 00888937017762; Part Numbers: 64-600

Where was it sold?

Worldwide distribution - US Nationwide and the countries of Armenia, Bahrain, Canada, Hong Kong, India, New Zealand, Qatar, Sweden.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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