Recall Z-0398-2023— Carefusion 2200 Inc

Name: FDA recall Z-0398-2023
Creator: U.S. Food and Drug Administration
Published: 2022-11-02

Class II · Ongoing

Class II FDA medical device recall by Carefusion 2200 Inc, initiated 2022-11-02. It names one FDA 510(k) clearance: K213386. Product: CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS, 0.7MM TIP OVERALL LENGTH 9-1/2" (240MM) , REF F-5008. Reason: XXX.

Recalling firm: Carefusion 2200 Inc
Classification: Class II
Status: Ongoing
Initiated: 2022-11-02
Firm location: Vernon Hills, IL, United States

510(k) clearances named in this recall

1 on FDA's record

K213386 — Titan Manufacturing Bipolar ForcepsTitan Manufacturing, Inc.·cleared 2021-10-25

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS, 0.7MM TIP OVERALL LENGTH 9-1/2" (240MM) , REF F-5008

Reason for recall

XXX

Data sourced from openFDA. This site is unofficial and independent of the FDA.