FDA recall record

CooperSurgical Wallace Artificial Insemination Catheter, 180 mm, Sterile, Quantity: 1 Box recall — FDA Z-1713-2020

Expiration date discrepancy. Marked as 5 years. Expiration date should be 3 years.

Class IIIclassification
Z-1713-2020official record ID
Apr 22, 2020report date

Recall record at a glance

Official recordZ-1713-2020
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmCooperSurgical, Inc.
Report dateApr 22, 2020
Recall initiation dateFeb 28, 2020
LocationTrumbull, CT, United States

Official product description

Wallace Artificial Insemination Catheter, 180 mm, Sterile, Quantity: 1 Box (10 units), Model: AIC18JP, Cooper Surgical Inc., (01) 2 0888937 021749 - Product Usage: Intended use of the product is the introduction of washed spermatozoa into the uterine cavity.

Why the product was recalled

Expiration date discrepancy. Marked as 5 years. Expiration date should be 3 years.

Distribution information

International distribution to Japan only.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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