Product Recalls in Utah
Product recalls affecting Utah — including food, drugs, consumer products, medical devices, and vehicles distributed to Utah. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,627 recalls have been distributed to Utah in the last 12 months.
Showing 7441–7460 of 28,579 recalls
Recalled Item: CareFusion V. Mueller CUSHING BAYONET BIPOLAR INSULATED FORCEPS Recalled by...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carefusion V. Mueller" SCOVILLE-GREENWOOD BAYONET BIPOLAR FORCEPS 1.5MM TIP...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carefusion V. Mueller JEWELERS BIPOLAR FORCEPS 0.4MM TIP Recalled by...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carefusion V. Mueller HARDY BAYONET BIPOLAR FORCEPS WITH STOP Recalled by...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS 1.5MM...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carefusion V. Mueller GERALD BAYONET IRRIGATING BIPOLAR FORCEPS 1.0MM TIP...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS 0.7MM...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion V. Mueller TITANIUM BAYONET BIPOLAR FORCEPS Recalled by...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion V. Mueller Neuro/Spine TITANIUM BAYONET INSULATED IRRIGATING...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion V. Mueller TITANIUM BAYONET IRRIGATING BIPOLAR FORCEPS INSULATED...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion V. Mueller Neuro/Spine TITANUIM BIPOLAR FORCEPS STRAIGHT Recalled...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm LifePort Endotracheal Tube Adapters 10-pack Recalled by Bunnell, Inc....
The Issue: Some adaptors, for use with high frequency ventilators, were packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion V. Mueller ROUND HANDLE BAYONET BIPOLAR FORCEPS Recalled by...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS Recalled...
The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The FAST System and the FAST PBC Prep Cartridge together are a closed...
The Issue: Device exceeds the limitations of a Class I 510(k)-exempt device so the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Custom Surgical Instrument Disposable Kits: Part Numbers / Product...
The Issue: Due to Customer Convenience Kits containing 3M Steri-Drape Surgical Drapes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE MAGEC MAGEC 2 Rod. The MAGEC System is used Recalled by NuVasive...
The Issue: During accelerated shelf-life extension studies it was noted that the final...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 Recalled by...
The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IgM Immunoturbidimetric Assay-In vitro determination of IgA and IgM in...
The Issue: Update to the carryover avoidance technical bulletin to detail that IgA and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IgA Immunoturbidimetric Assay- In vitro determination of IgA and IgM...
The Issue: Update to the carryover avoidance technical bulletin to detail that IgA and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.