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. 2,595 recalls have been distributed to Arizona in the last 12 months.
Showing 22341–22360 of 52,339 recalls
Recalled Item: GENCONTUSS (Chlorpheniramine Maleate Recalled by Pharma-Natural Inc. Due to...
The Issue: CGMP Deviations: products were manufactured with lack of process validation,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AbeeMed cream (Menthol 1.48% and Histamine DHCL 0.05%) Recalled by...
The Issue: CGMP Deviations: products were manufactured with lack of process validation,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ARMY HEALTH With CURCUMIN (Menthol 3.00%) Pain Reliever Roll-On Recalled by...
The Issue: CGMP Deviations: products were manufactured with lack of process validation,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NEOGEN-D (Dextromethorphan HBr Recalled by Pharma-Natural Inc. Due to CGMP...
The Issue: CGMP Deviations: products were manufactured with lack of process validation,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DOUBLE TUSSIN DM (Dextromethorphan Hbr 20 mg Recalled by Pharma-Natural Inc....
The Issue: CGMP Deviations: products were manufactured with lack of process validation,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ARMY HEALTH Pain Reliever Gel With CURCUMIN (Menthol 3.00%) Recalled by...
The Issue: CGMP Deviations: products were manufactured with lack of process validation,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oliver's Harvest CBD+Lidocaine HCL 4% Pain Relief (Lidocaine HCL 4%)...
The Issue: CGMP Deviations: products were manufactured with lack of process validation,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lid O Creme (Lidocaine HCL 4% and Menthol 1%) Topical Analgesic Cream...
The Issue: CGMP Deviations: products were manufactured with lack of process validation,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dayma SUPER FORTE XL10 (Camphor 0.5% Recalled by Pharma-Natural Inc. Due to...
The Issue: CGMP Deviations: products were manufactured with lack of process validation,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lido E.R. (Lidocaine HCL 4%) Pain Relieving Topical Analgesic Cream Recalled...
The Issue: CGMP Deviations: products were manufactured with lack of process validation,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SORBUGEN NR (Dextromethorphan HBr Recalled by Pharma-Natural Inc. Due to...
The Issue: CGMP Deviations: products were manufactured with lack of process validation,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: A&E Medical Corp. Ultra-Flex MYO/Wire Ultra-Flex Monopolar Pacing Wire...
The Issue: Updated instructions for use: Ultra-Flex MYO/WIRE Monopolar pacing wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norm-O-Temp model 111Z Recalled by Cincinnati Sub-Zero Products LLC, a...
The Issue: The manual does not provide instruction stating that exceeding 40 Celsius...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE DR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Norm-O-Temp model 111W Recalled by Cincinnati Sub-Zero Products LLC, a...
The Issue: The manual does not provide instruction stating that exceeding 40 Celsius...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELLIPSE VR Recalled by St Jude Medical Inc. Due to Electrical failures were...
The Issue: Electrical failures were identified in cardioverter defibrillators (ICDs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.