JAGTOME RX 39-20-260-025 Material Number: M00573080 — Class II medical device recall Z-0768-2022
Ongoing recall by Boston Scientific Corporation, reported 2022-03-23, distributed nationwide. Sterility of device is compromised due to a sterile barrier breach
| Recall number | Z-0768-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Boston Scientific Corporation, Marlborough, MA, United States |
| Recall initiated | 2021-12-22 |
| Classified | 2022-03-11 |
| Reported by FDA | 2022-03-23 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, BE, CA, CH, CN, CZ, DE, DK, ES, FI, FR, GB, GR, IE, IT, JP, KR, KW, LB, LV, MA, NL, NO, NZ, PL, PT, QA, RO, SA, SE, SI, SK, ZA |
| Quantity | 4,487 units |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 08714729776642 |
| Lot numbers | 27505913, 27563424, 27629942, 27731957, 27755861, 27839657, 27846391, 27986551, 27991931, 28036372 |
Product
JAGTOME RX 39-20-260-025 Material Number: M00573080
Reason for recall
Sterility of device is compromised due to a sterile barrier breach
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-0768-2022. 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.