FDA Device recall Z-1713-2020
Wallace Artificial Insemination Catheter, 180 mm, Sterile, Quantity: 1 Box (10 units), Model: AIC18JP, Cooper Surgical Inc., (01) 2 0888937…
- FDA Device
- Class III
- terminated
- Published 2020-04-22
On 2020-04-22 the FDA classified a Class III recall of Wallace Artificial Insemination Catheter, 180 mm, Sterile, Quantity: 1 Box (10 units), Model: AIC18JP, Cooper Surgical Inc., (01) 2 0888937… by Coopersurgical, citing expiration date discrepancy. Marked as 5 years. Expiration date should be 3 years.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1713-2020 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2020-02-28 |
| Published | 2020-04-22 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Coopersurgical |
| Distribution | n/a |
Product
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.
Reason
Expiration date discrepancy. Marked as 5 years. Expiration date should be 3 years.
Identifiers
| code_info | Lot number 250887 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1713-2020%22
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