Medtronic DPL Single Stage Venous Cannula with Metal Tip — Class II medical device recall Z-0908-2013
Terminated recall by Medtronic Inc. Cardiac Rhythm Disease Management, reported 2013-03-13, distributed nationwide. Potential for uncharacteristically rough metal edges to occur along the inner diameter of the metal tip side p
| Recall number | Z-0908-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Inc. Cardiac Rhythm Disease Management, Saint Paul, MN, United States |
| Recall initiated | 2013-02-19 |
| Classified | 2013-03-05 |
| Reported by FDA | 2013-03-13 |
| Terminated | 2013-11-21 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, AT, AU, BE, BR, CA, CH, CL, CO, CY, CZ, DE, DK, DZ, EC, EG, ES, FI, FR, GB, GR, GT, HK, HR, HU, ID, IE, IL, IN, IT, JM, JP, KR, LT, MA, MX, MY, NL, NO, NZ, PE, PH, PL, PT, QA, RO, SA, SE, SG, TH, TR, TW, VN, ZA |
| Lot numbers | 2012090236, 2012090239, 2012090240, 2012090293, 2012090294, 2012090296, 2012090337, 2012090389, 2012090416, 2012090435, 2012090571, 2012090572, 2012090854, 2012090855, 2012091024, 2012091222, 2012100039, 2012100040, 2012100041, 2012100086, 2012100087, 2012100107, 2012100161, 2012100905, 2012101346, 2012110007, 2012110008, 2012110010, 2012110030, 2012110144, 2012110184, 2012110251, 2012110252, 2012110326, 2012110327, 2012110394, 2012110395, 2012110396, 2012110767, 2012110850 and 78 more |
| Model numbers | 2012090236, 2012090239, 2012090240, 2012090293, 2012090294, 2012090296, 2012090337, 2012090389, 2012090416, 2012090435, 2012090571, 2012090572, 2012090854, 2012090855, 2012091024, 2012091222, 2012100039, 2012100040, 2012100041, 2012100086, 2012100087, 2012100107, 2012100161, 2012100905, 2012101346 and 93 more |
Product
Medtronic DPL Single Stage Venous Cannula with Metal Tip, used in cardiopulmonary bypass procedures. Model numbers: 67312; 67314; CB67314; 67316; 67318; CB67318; 67320; 69312; 69314; 69316; 69318; 69320; 69322; 69324; 69328; 69331.
Reason for recall
Potential for uncharacteristically rough metal edges to occur along the inner diameter of the metal tip side ports of the cannula.
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-0908-2013. 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.