0 — Class II medical device recall Z-2670-2014
Terminated recall by Centurion Medical Products Corporation, reported 2014-10-01, distributed in AZ, CA, IA, IL, IN, MA, MD, NC…. Unit packages may exhibit open seals which impacts package integrity and potentially product sterility.
| Recall number | Z-2670-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Centurion Medical Products Corporation, Williamston, MI, United States |
| Recall initiated | 2014-07-25 |
| Classified | 2014-09-19 |
| Reported by FDA | 2014-10-01 |
| Terminated | 2014-11-25 |
| Distributed | AZ, CA, IA, IL, IN, MA, MD, NC, NE, NY, OK, OR, PA, SD, TN, TX, UT, VA, WA, WI |
| Quantity | 21,388 |
| Reason classes | sterility, packaging |
| Lot numbers | 2013040180, 2013050680, 2013051380, 2013052080, 2013052880, 2013061080, 2013061780, 2013062480, 2013072980, 2013081350, 2013081550, 2013081950, 2013082050, 2013082150, 2013082850, 2013082950, 2013091250, 2013091750, 2013091950, 2013092450, 2013092650, 2013102880, 2013111180, 2013111880, 2013120280, 20CM, 3024261, 3046276, 4128353, CVI3240/PORT, CVI3425/CVC, CVI3525/UNIVERSAL, CVI3535/CENTRAL, DT10560/INFUSION, DT10620/FISTULAKIT, DT11270/VADKIT, DT11390/ONCOLOGY, DT11395/ONCOLOGY, DT12955/UNIVERSAL, DT13610/PICC and 20 more |
| Model numbers | 306553 |
Product
0.9% Sodium Chloride Injection, USP BD PosiFlush(TM) SF Saline Flush Syringe 10 mL REF#306553 used in Centurion Convenience Kits. Recalled product is attached to the outside of the Convenience Kits.
Reason for recall
Unit packages may exhibit open seals which impacts package integrity and potentially product sterility.
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-2670-2014. 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.