Centurion Medical Products UNIVERSAL LINE FULL BODY DRAPE KIT — Class II medical device recall Z-0344-2020
Terminated recall by Centurion Medical Products Corporation, reported 2019-11-13, distributed nationwide. Sterile packaging incomplete seals may compromise sterility of the product
| Recall number | Z-0344-2020 |
|---|---|
| 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 | 2019-10-24 |
| Classified | 2019-11-06 |
| Reported by FDA | 2019-11-13 |
| Terminated | 2020-06-24 |
| Distributed | Nationwide (US) |
| Quantity | 80 units |
| Reason classes | sterility |
| Lot numbers | 2019052190 |
| Expiration dates | 2024-05-31 |
Product
Centurion Medical Products UNIVERSAL LINE FULL BODY DRAPE KIT - REG Code: DT11955
Reason for recall
Sterile packaging incomplete seals may compromise sterility of the product
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-0344-2020. 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.