Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2416-2023 — Snowden-Pencer MIS DIAMOND-TOUCH GRASPER DIAMOND JAW BABCOCK 5MM, 32CM, RATCHETED, REF SP90-7018; endoscopic surgical device

U.S. FDA — Device Enforcement · United States · 2023-07-13 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2416-2023
Date of alert
2023-07-13
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Carefusion 2200 Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10885403159701
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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