Product Recalls in Arizona
Product recalls affecting Arizona — including food, drugs, consumer products, medical devices, and vehicles distributed to Arizona. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,759 recalls have been distributed to Arizona in the last 12 months.
Showing 7381–7400 of 29,154 recalls
Recalled Item: Medical Action INDUSTRIES INC. Port a Cath Kit Recalled by Medical Action...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests OUS...
The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests (600T)-...
The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VADER Pedicle System Torque Wrench Recalled by Icotec Ag Due to During...
The Issue: During internal testing (at manufacturer site) of two torque wrench devices,...
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 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 TITANIUM BAYONET INSULATED IRRIGATING BIPOLAR FORCEPS...
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 JEWELERS BIPOLAR FORCEPS 0.4MM 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 ROUND HANDLE BAYONET 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 SCOVILLE-GREENWOOD BAYONET BIPOLAR FORCEPS 1.5MM TIPS...
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 ADSON BIPOLAR FORCEPS 1.0MM TIP OVERALL LENGTH...
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 euro/Spine TITANIUM ROUND HANDLE BAYONET BIPOLAR...
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: 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: SynCardia Total Artificial Heart System (70CC): 500101-001 SynCardia Total...
The Issue: Due to tears reported tears in the cannula due to wear and tear stress.
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 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: 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 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.