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. 1,096 recalls have been distributed to Arizona in the last 12 months.
Showing 13141–13160 of 52,339 recalls
Recalled Item: 23.4% Sodium Chloride Injection Recalled by The Ritedose Corporation Due to...
The Issue: Labeling: Incorrect Barcode: Product barcode incorrectly identifies the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cequa (cyclosporine ophthalmic solution) 0.09% Recalled by SUN...
The Issue: Subpotent Drug and Presence of Particulate Matter: low out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CBD Metered Dose Inhaler (CBD) 5 mg Dose Recalled by Wellness BioSciences...
The Issue: Marketed Without an Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets USP Recalled by Lupin...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets USP Recalled by Lupin...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Janumet (sitagliptin and metformin HCl) tablets Recalled by MERCK SHARP &...
The Issue: Presence of foreign substance: Presence of stainless steel particulates in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets USP Recalled by Lupin...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olympus DISPOSABLE GRASPING FORCEPS Recalled by Olympus Corporation of the...
The Issue: Forceps do not comply with Olympus standards for the amount of force...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical H/S CATHETER SET FR 5 with Integated Stylet Model: Recalled...
The Issue: Incorrect bonding material used for assembly of the catheter, may fail,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical H/S ELLIPTOSPHERE CATH 5 Fr -For administering contrast...
The Issue: Incorrect bonding material used for assembly of the catheter, may fail,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical H/S ELLIPTOSPHERE CATH 5 FR Set-For administering contrast...
The Issue: Incorrect bonding material used for assembly of the catheter, may fail,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triathlon Tritanium Tibial Component (Size 6) Recalled by Howmedica...
The Issue: Stryker has discovered a potential product mix where the size of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroMARK Breast Biopsy Marker Recalled by Devicor Medical Products Inc Due...
The Issue: Small patient labels do not match the primary device label. The primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dragonfly OpStar Imaging Catheter Recalled by Abbott Vascular Due to There...
The Issue: There is a potential that the proximal marker may separate from the imaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percept BrainSense Implantable Neurostimulator (INS) Recalled by Medtronic...
The Issue: The Implantable Neurostimulator (INS) cannot communicate with the clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use Recalled by Medtronic Inc Due to Errors and...
The Issue: Errors and inconsistencies that were identified in the Instruction for Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare TDX SP2 Recalled by Invacare Corporation Due to The battery wiring...
The Issue: The battery wiring harness on affected wheelchairs may become disconnected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.