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. 2,562 recalls have been distributed to Arizona in the last 12 months.
Showing 31941–31960 of 52,339 recalls
Recalled Item: Sargento Sliced Red Rind Munster Cheese Recalled by Sargento Foods, Inc. Due...
The Issue: Sargento Foods Inc. was notified by their supplier that the cheese that was...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sargento Chef Blends Shredded Taco Cheese Recalled by Sargento Foods, Inc....
The Issue: Sargento Foods Inc. was notified by their supplier that the cheese that was...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Olympus ENDOEYE HD II Video Telescopes Models: WA50040A Endoeye HD II...
The Issue: A damaged temperature sensor at the endoscope's tip can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire Recalled by...
The Issue: CSI is recalling three lots of VIPERWIRE ADVANCE WITH FLEXTIP PERIPHERAL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Recalled by Remel Inc Due to Test organisms exhibit poor growth when...
The Issue: Test organisms exhibit poor growth when grown using the test agar. The poor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ibuprofen Lysine Injection Recalled by X-Gen Pharmaceuticals Inc. Due to...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CycloSPORINE Capsules Recalled by Amerisource Health Services Due to Failed...
The Issue: Failed Impurities/Degradations Specifications; out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SharkCore Fine Needle Biopsy System (25GA) Recalled by Medtronic Due to...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arkon Anesthesia Delivery System Recalled by Del Mar Reynolds Medical, Ltd....
The Issue: Spacelabs has received reports of the Arkon Anesthesia Delivery System,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BNX Fine Need Aspiration System (19GA) Recalled by Medtronic Due to Handle...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SharkCore Fine Needle Biopsy System (22 GA) Recalled by Medtronic Due to...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SharkCore LG Fine Needle Biopsy System (19GA) Recalled by Medtronic Due to...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BNX Fine Need Aspiration System (22GA) Recalled by Medtronic Due to Handle...
The Issue: Handle may break during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg Recalled by Teva...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levofloxacin Ophthalmic Solution Recalled by Actavis Inc Due to Failed...
The Issue: Failed Impurities/ Degradation Specifications: OOS for related compound...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xanthium & Siler Combo (Bi Yan Pian) DIETARY SUPPLEMENT Recalled by Kingsway...
The Issue: Presence of Ephedrae Herba (ma huang), a FDA Banned Ephedra Alkaloid
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Raindrop Near Vision Inlay Recalled by Revision Optics Inc Due to ReVision...
The Issue: ReVision Optics has updated the instructions for use (IFU) for the Raindrop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Stiffer Catheter with...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (paper...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Cholangiogram Catheter with introducer(eIFU) REF #...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.