Multi-Med Single Lumen Catheters sold in Centurion convenience kits — Class I medical device recall Z-0647-2017
Terminated recall by Centurion Medical Products Corporation, reported 2016-12-14, distributed nationwide. The kits contain Multi-Med Single Lumen Catheters that have a potential for excess material to remain at the t
| Recall number | Z-0647-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Centurion Medical Products Corporation, Williamston, MI, United States |
| Recall initiated | 2016-10-21 |
| Classified | 2016-12-02 |
| Reported by FDA | 2016-12-14 |
| Terminated | 2017-07-20 |
| Distributed | Nationwide (US) |
| Quantity | 1,000 kits |
| Lot numbers | 2016050950, 2016051050, 2016052050, 2016053150, 2016060750, 2016060850, 2016061550, 2016061650, 2016062050, 2016062150, 2016062850, 2016062950, 2016063050, 2016070550, 2016070650, 2016071250, 2016071350, 2016071950, 2016072050, 2016072650, 2016072950, 2016080250, 2016080350, 2016081550, 2016082350, 2016082450, 2016082650, 2016082950, 2016090250, 2016090750, 2016091950, 2016092650, 2016093050, 2016100650, 2016101050 |
Product
Multi-Med Single Lumen Catheters sold in Centurion convenience kits. The Multi-Med catheter is indicated for use in patients requiring administration of solutions, blood sampling, and central venous pressure monitoring.
Reason for recall
The kits contain Multi-Med Single Lumen Catheters that have a potential for excess material to remain at the tip of the catheter from the manufacturing process. It is possible that the excess material may separate from the catheter during use and pose a potential risk of embolism, which could result in serious injury or death.
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-0647-2017. 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.