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. 2,406 recalls have been distributed to Arizona in the last 12 months.
Showing 51941–51960 of 52,339 recalls
Recalled Item: Eloxatin (OXALIplatin injection) 5 mg/mL Injection Recalled by...
The Issue: CGMP Deviations: Eloxatin was manufactured by Ben Venue Laboratories, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eloxatin (OXALIplatin injection) 5 mg/mL injection Recalled by...
The Issue: CGMP Deviations: Eloxatin was manufactured by Ben Venue Laboratories, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CaviCide Recalled by Metrex Research, LLC. Due to Metrex Research is...
The Issue: Metrex Research is recalling Cavicide containing the Spring Fresh Fragrance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerifyNow P2Y12 Assay Recalled by Accumetrics Inc Due to The recall was...
The Issue: The recall was initiated by Accumetrics because of a field correction to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerifyNow System Recalled by Accumetrics Inc Due to The recall was initiated...
The Issue: The recall was initiated by Accumetrics because of a field correction to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+3 Infusion Pump System Recalled by Hospira Inc. Due to Hospira has...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Hyperbaric Infusion Pump Recalled by Hospira Inc. Due to Hospira has...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...
The Issue: Hospira has received reports of distal pressure sensor calibration drift on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: "****ORTHO SENSOR**12-123-A Knee Trial for Trithion***1560 Saw grass...
The Issue: Ortho sensor in Sunrise, FL is recalling the Graphics User Interface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thyro-Tab 0.050mg. Recalled by Lloyd Inc Due to Subpotent (Single Ingredient...
The Issue: Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc Due to...
The Issue: Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: COBAS AmpliPrep Sample Tube Input Barcode Clips Recalled by Roche Molecular...
The Issue: Certain lots of COBAS AmpliPrep (CAP) S-tube Input (Box of 12 bags 12x24...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-Stat BNP cartridges Abbott Point of Care Inc. The i-Stat Recalled by...
The Issue: The frequency of suppressed results for i-Stat cTnl, BNP and CK-MP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-Stat CK-MP cartridges Abbott Point of Care Inc. The i-Stat Recalled by...
The Issue: The frequency of suppressed results for i-Stat cTnl, BNP and CK-MP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-Stat cTnl cartridges Abbott Point of Care Inc. The i-Stat Recalled by...
The Issue: The frequency of suppressed results for i-Stat cTnl, BNP and CK-MP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMAGE Immunochemistry Systems Rheumatoid Factor (RF) Reagent Recalled by...
The Issue: The recall was initiated because Beckman Coulter has confirmed customer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.