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. 1,122 recalls have been distributed to Arizona in the last 12 months.
Showing 7941–7960 of 52,339 recalls
Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stabilyze Sugar Stable Dark Chocolate Peanut Butter Recalled by Betty Lou's...
The Issue: Undeclared Sesame
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Frozen and fresh RTE Lobster meat (1 lb. packages to Recalled by Greenhead...
The Issue: Lobster meat may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: D-Clip Standard/Mini Applier Recalled by Peter Lazic Gmbh Due to Customer...
The Issue: Customer complaint received that reported the applier failed during surgery....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-Clip Standard/Mini Applier Recalled by Peter Lazic Gmbh Due to Customer...
The Issue: Customer complaint received that reported the applier failed during surgery....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORION System with software OSS v6.0 and OSS v7.0- An Recalled by LEONI CIA...
The Issue: Users of the patient positioning system ORION System can be faced with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-Clip Standard/Mini Applier Recalled by Peter Lazic Gmbh Due to Customer...
The Issue: Customer complaint received that reported the applier failed during surgery....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORION System with software OSS v6.0 and OSS v7.0- An Recalled by LEONI CIA...
The Issue: Users of the patient positioning system ORION System can be faced with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Encore Medical, LP Due to Mislabeling
The Issue: Mislabeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobilett Mira wireless (VA20) mobile x-ray system(s) Recalled by Siemens...
The Issue: Due to the incorrect mounting of the buzzer component, there is no acoustic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CereLink ICP Extension Cable (Extension Cable) Recalled by Integra...
The Issue: Firm is expanding the existing recall RES 90457 for the Cerelink, initiated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reverse Shoulder System e+ Recalled by Encore Medical, LP Due to Mislabeling
The Issue: Mislabeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Certain Over-The-Counter (OTC) drug products sold by Family Dollar retail...
The Issue: CGMP Deviations: OTC products were stored outside of labeled temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MEDFLEX Recalled by CareFusion 303, Inc. Due to If "Clear All" selected...
The Issue: If "Clear All" selected medications is selected on patient profile, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Uric Acid Monitoring System Each kit contains 1 meter Recalled by...
The Issue: Due to products distributed without premarket clearance or approvals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Uric Acid Monitoring System Each kit contains 1 meter Recalled by...
The Issue: Due to products distributed without premarket clearance or approvals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxytocin synthetic Recalled by Denver Solutions, LLC DBA Leiters Health Due...
The Issue: Labeling: Not Elsewhere Classified
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bupropion Hydrochloride Extended-Release Tablets USP (SR) Recalled by SUN...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VANCOmycin HCI PF Recalled by Denver Solutions, LLC DBA Leiters Health Due...
The Issue: Labeling: Not Elsewhere Classified
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.