Snowden-Pencer MIS DIAMOND-TOUCH DISSECTOR FENESTRATED 16MM JAW 5MM — Class II medical device recall Z-2418-2023
Ongoing recall by Carefusion 2200 Inc, reported 2023-08-23. Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to th
| Recall number | Z-2418-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Carefusion 2200 Inc, Vernon Hills, IL, United States |
| Recall initiated | 2023-07-13 |
| Classified | 2023-08-17 |
| Reported by FDA | 2023-08-23 |
| Countries outside the US | CA |
| Quantity | 0 units |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 10885403159862 |
| Lot numbers | B23 |
| Model numbers | P90-7036 |
Product
Snowden-Pencer MIS DIAMOND-TOUCH DISSECTOR FENESTRATED 16MM JAW 5MM, 32CM, NON RATCHETED, REF SP90-7036; endoscopic surgical device
Reason for recall
Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.
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-2418-2023. 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.