Y-CONNECTOR: 6" Small Kink Resistant Tubing Bifurcated Connector /2… — Class II medical device recall Z-0195-2023
Terminated recall by Avanos Medical, Inc., reported 2022-11-16, distributed in CA, CO, FL, MI, NM, OH, OR, TN…. Sterile extension sets were distributed without an expiration date
| Recall number | Z-0195-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Avanos Medical, Inc., Alpharetta, GA, United States |
| Recall initiated | 2022-09-14 |
| Classified | 2022-11-07 |
| Reported by FDA | 2022-11-16 |
| Terminated | 2023-08-31 |
| Distributed | CA, CO, FL, MI, NM, OH, OR, TN, TX, UT, WI |
| Quantity | 1,378 units |
| Reason classes | sterility |
| Model numbers | 220227, BC-006-04, BC00604 |
Product
Y-CONNECTOR: 6" Small Kink Resistant Tubing Bifurcated Connector /2 Male Luer Locks, 1 Female Luer Lock, Labeled as: SUMMIT MEDICAL PRODUCTS, REF 220227; MPS Acacia CAT NO: BC-006-04; MEDICAL PRODUCTS SPECIALISTS EXTENSION SET, Catalog Number BC00604, pain control pump accessory
Reason for recall
Sterile extension sets were distributed without an expiration date
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-0195-2023. 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.