Name: Pasteur Pipets — Class II medical device recall Z-1946-2014
Terminated recall by ORIGIO, Inc, reported 2014-07-09, distributed nationwide. Identification of packaging breach of the nylon pouch sterile barrier for the 3-pack configuration
| Recall number | Z-1946-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ORIGIO, Inc, Charlottesville, VA, United States |
| Recall initiated | 2014-06-20 |
| Classified | 2014-06-30 |
| Reported by FDA | 2014-07-09 |
| Terminated | 2015-07-20 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AU, BB, CA, CL, CN, CO, DE, DK, EC, ES, FR, GB, GR, IN, IT, JO, JP, MY, NL, PE, RU, SG, TR, TW, ZA |
| Reason classes | sterility |
| Model numbers | PP-5.75-90, PP-5.75-90PL, PP-9-90, PP-9-90PL |
| Expiration dates | 2015-05-02 |
Product
Name: Pasteur Pipets, used by the embryologist in the IVF Laboratory. Model numbers: PP-5.75-90 PP-9-90 PP-5.75-90PL PP-9-90PL
Reason for recall
Identification of packaging breach of the nylon pouch sterile barrier for the 3-pack configuration
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-1946-2014. 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.