Vial2BAG DC 20mm: 1) REF 6070112 & 2) REF 6070112C — Class I medical device recall Z-0769-2019
Terminated recall by WEST PHARMA. SERVICES IL, LTD, reported 2019-02-06. Adverse events have been reported with the use of oxytocin in conjunction with the 13mm Vial2Bag DC in pregnan
| Recall number | Z-0769-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | WEST PHARMA. SERVICES IL, LTD, Ra'Anana, N/A, Israel |
| Recall initiated | 2018-12-26 |
| Classified | 2019-01-28 |
| Reported by FDA | 2019-02-06 |
| Terminated | 2022-07-20 |
| Quantity | 30 million |
| UPC / GTIN / UDI-DI | 07290108240054, 07290108241006 |
| Lot numbers | 7689, 7690, 7750, 7751, 7865, 7866, 7867, 7868, 7886, 7887, 7888, 7900, 7901, 7902, 7949, 7951, 7952, 7954, 7957, 7958, 7959, 7960, 8019, 8020, 8021, 8022, 8132, 8133, 8134, 8135, 8136, 8137, 8138, 8139, 8140, 8141, 8142, 8143, 8144, 8145 and 405 more |
| Model numbers | 6070112, 6070112C |
Product
Vial2BAG DC 20mm: 1) REF 6070112 & 2) REF 6070112C, Single use only, Rx Only
Reason for recall
Adverse events have been reported with the use of oxytocin in conjunction with the 13mm Vial2Bag DC in pregnant women. Vial2Bag DC 20mm is recalled due to similarities with 13mm Vial2Bag DC.
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-0769-2019. 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.