ONE-LINK NON-DEHP Y-TYPE MICROBORE CATHETER EXTENSION SET NEEDLE-FREE… — Class II medical device recall Z-0132-2016
Terminated recall by Baxter Healthcare Corp, reported 2015-10-28. Potential for a leak at the tubing to luer bond.
| Recall number | Z-0132-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corp, Deerfield, IL, United States |
| Recall initiated | 2015-05-21 |
| Classified | 2015-10-16 |
| Reported by FDA | 2015-10-28 |
| Terminated | 2017-05-10 |
| Quantity | 23,600 |
| Reason classes | packaging |
| Lot numbers | UR15B16021, UR15B23043 |
Product
ONE-LINK NON-DEHP Y-TYPE MICROBORE CATHETER EXTENSION SET NEEDLE-FREE IV CONNECTOR WITH NEUTRAL FLUID DISPLACEMENT
Reason for recall
Potential for a leak at the tubing to luer bond.
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-0132-2016. 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.