Adult Divided Cannula end tidal C)2 sampling w/male luer-lock… — Class II medical device recall Z-1898-2012
Terminated recall by SALTER LABS, reported 2012-07-04, distributed nationwide. A complaint was received, and later verified, that product labeled as SO-1296 with male luer lock connector ac
| Recall number | Z-1898-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | SALTER LABS, Arvin, CA, United States |
| Recall initiated | 2012-05-30 |
| Classified | 2012-06-27 |
| Reported by FDA | 2012-07-04 |
| Terminated | 2012-07-27 |
| Distributed | Nationwide (US) |
| Quantity | 242 cases |
| Reason classes | labeling |
| Lot numbers | 032612 |
| Model numbers | SO-1296 |
Product
Adult Divided Cannula end tidal C)2 sampling w/male luer-lock connector. 7 ft, oxygen tube, 7 ft. CO2 tube RX only.For Single Patient Use only. Distributed by Tri-Anium Assembled in Mexico. Usage: Delivery of Anesthesia.
Reason for recall
A complaint was received, and later verified, that product labeled as SO-1296 with male luer lock connector actually contained product with a female luer lock connector.
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-1898-2012. 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.