Wallace Artificial Insemination Catheter — Class III medical device recall Z-1713-2020
Terminated recall by CooperSurgical, Inc., reported 2020-04-22. Expiration date discrepancy. Marked as 5 years. Expiration date should be 3 years.
| Recall number | Z-1713-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CooperSurgical, Inc., Trumbull, CT, United States |
| Recall initiated | 2020-02-28 |
| Classified | 2020-04-15 |
| Reported by FDA | 2020-04-22 |
| Terminated | 2020-08-11 |
| Countries outside the US | JP |
| Lot numbers | 250887 |
| Model numbers | AIC18JP |
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 for recall
Expiration date discrepancy. Marked as 5 years. Expiration date should be 3 years.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1713-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.