FDA Device recall Z-1946-2014
Name: Pasteur Pipets, used by the embryologist in the IVF Laboratory
- FDA Device
- Class II
- terminated
- Published 2014-07-09
On 2014-07-09 the FDA classified a Class II recall of Name: Pasteur Pipets, used by the embryologist in the IVF Laboratory by Origio, citing identification of packaging breach of the nylon pouch sterile barrier for the 3-pack configuration.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1946-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-06-20 |
| Published | 2014-07-09 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Origio |
| Distribution | US |
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
Identification of packaging breach of the nylon pouch sterile barrier for the 3-pack configuration
Identifiers
| code_info | CODE: Model #s: PP-5.75-90, PP-9-90, PP-5.75-90PL, PP-9-90PL. Lots with labeled expiry date of May 2, 2015, or later. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1946-2014%22
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