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. 2,458 recalls have been distributed to Arizona in the last 12 months.
Showing 36621–36640 of 52,339 recalls
Recalled Item: Capecitabine tablets USP 500 mg Recalled by Teva North America Due to Failed...
The Issue: Failed Dissolution Specifications: low test results at the 18 month time-point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chocolate Marshmallows Recalled by Zingerman's Candy Manufactory Due to...
The Issue: Product recalled due to undeclared soy.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Zzang! Original Candy Bar Recalled by Zingerman's Candy Manufactory Due to...
The Issue: Product recalled due to undeclared soy and milk (butter declared).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Zzang! Wowza Candy Bar Recalled by Zingerman's Candy Manufactory Due to...
The Issue: Product recalled due to undeclared soy; and undeclared milk (cream declared).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Zzang! Cashew Cow Candy Bar Recalled by Zingerman's Candy Manufactory Due to...
The Issue: Product recalled due to undeclared sub-ingredient soy.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Zzang! Holiday 4 pack Candy Bars Recalled by Zingerman's Candy Manufactory...
The Issue: Product recalled due to undeclared soy; and undeclared allergen milk (cream...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hip Preservation System Signature Series PreBent Burs under the following...
The Issue: Metal shavings released from burs during use are due to contact between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Concerto Basic Shower Trolley is intended for assisted hygiene care...
The Issue: Reports of the bolts connecting the stretcher to the hydraulic piston and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEL- GBS Medium (Broth 3 ml Fill 13 x 100 mm Screw Cap Tube Catalog No.:...
The Issue: Product marketed without a 510 (k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEL GBS Medium 20 ml in 100x15mm plate (Standard Petri Dish) Catalog No.:...
The Issue: Product marketed without a 510 (k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The THERAKOS CELLEX Photopheresis System is a photoimmune therapy. Catalog...
The Issue: The Mallinckrodt (Therakos) post-market monitoring process detected an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Increased U90-382 or...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 350 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 250 Chemistry Systems Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Increased U90-382 or 6LU condition codes generated by VITROS 250, 350, 5,1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Recalled by Baxter Corporation Englewood Due to All lots of RAPIDFILL...
The Issue: All lots of RAPIDFILL Syringe Strips lack evidence supporting the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Life-Line DOCUSATE CALCIUM Sodium Free STOOL SOFTENER 240 mg each Recalled...
The Issue: Labeling: Label mix-up. Docusate Sodium 100mg Softgels were mislabeled as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BARDEX I.C. Anti-Infective 2-Way 5cc Foley Catheter. Intended for urinary...
The Issue: Labeling error: Catalog contains Instructions for Use (IFU) error; incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARDEX I.C. Anti-Infective 2-Way 3cc Foley Catheter Recalled by C.R. Bard,...
The Issue: Labeling error: Catalog contains Instructions for Use (IFU) error; incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.