FDAClass IIDecember 13, 2023

CooperSurgical H/S CATHETER SET FR 5 with Integated recall

CooperSurgical H/S CATHETER SET FR 5 with Integated Stylet Model: 61-4005S For administering contrast media during Hysterosalpingography or…

Why was CooperSurgical H/S CATHETER SET FR 5 with Integated recalled?

Incorrect bonding material used for assembly of the catheter, may fail, resulting in detachment of component parts, broken components, or leakage. This breakage may result in delay of procedure

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI-DI: 60888937016453 S/N: 309967

Product
CooperSurgical H/S CATHETER SET FR 5 with Integated Stylet Model: 61-4005S For administering contrast media during Hysterosalpingography or…
Recalling firm
CooperSurgical, Inc.
Quantity
90 units
Distribution
Nationwide Foreign: BELGIUM CANADA MALAYSIA NETHERLANDS SPAIN SWEDEN SWITZERLAND
Recall date
December 13, 2023
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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