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. 2,611 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,611 in last 12 months

Showing 1956119580 of 52,339 recalls

DrugMarch 11, 2020· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Pantoprazole Sodium Delayed-Release Tablets Recalled by Jubilant Cadista...

The Issue: CGMP Deviations: Presence of dark brown discoloration on edges of tablets

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 11, 2020· Merit Medical Systems, Inc.

Recalled Item: PreludeSYNC DISTAL Radial Compression Devices Recalled by Merit Medical...

The Issue: During the sterilization of radial compression devices, some of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2020· Boddingtons Plastics Ltd

Recalled Item: Endocuff Vision: models ARV 110 Recalled by Boddingtons Plastics Ltd Due to...

The Issue: Updated Instructions For Use- to contraindications and potential...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2020· Northgate Technologies, Inc.

Recalled Item: ACMI 9FR PROBE (E4-9F) Manufactured for Olympus Surgical Technologies...

The Issue: Investigation into a biocompatibility test discrepancy where a lot failed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2020· Northgate Technologies, Inc.

Recalled Item: Probe Recalled by Northgate Technologies, Inc. Due to As part of an...

The Issue: As part of an investigation into a biocompatibility test discrepancy where a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2020· Skytron, Div. The KMW Group, Inc

Recalled Item: SkyVision SDS System - Video Integration Model: GC-SDS-BSCB-200 - Product...

The Issue: Intermittent failure of a signal being sent to a monitor from the touch...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2020· Radiometer Medical ApS

Recalled Item: ABL800 FLEX Recalled by Radiometer Medical ApS Due to Analyzer's barcode...

The Issue: Analyzer's barcode reader misinterprets the contents of barcode label used...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS Immunodiagnostic Products TT4 Reagent Pack Recalled by Ortho Clinical...

The Issue: The specified reagent packs exhibit an increase in the frequency of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceMarch 10, 2020· Northgate Technologies, Inc.

Recalled Item: AUTOLITH URO-TCH 9FR PROBE 54CM Recalled by Northgate Technologies, Inc. Due...

The Issue: Investigation into a biocompatibility test discrepancy where a lot failed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2020· Boston Scientific

Recalled Item: Sensor Nitinol Wire with Hydrophilic Tip .038 3CM FLEX STR/150CM Recalled by...

The Issue: An increase in the rate of complaints for difficulty or inability to track...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2020· Abbott Gmbh & Co. KG

Recalled Item: ARCHITECT HAVAB G Reagent Kit. List Number 6L27 25. Recalled by Abbott Gmbh...

The Issue: An erroneous concentration value for hepatitis A virus was utilized during...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2020· Boston Scientific

Recalled Item: Contour VL Ureteral Stent Set 6FX22-30CM with .035 Sensor UPN: M006180156080...

The Issue: An increase in the rate of complaints for difficulty or inability to track...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2020· Sysmex America, Inc.

Recalled Item: The CF-70 instrument (product code: LXG Recalled by Sysmex America, Inc. Due...

The Issue: Software mismatch-When the software versions between the SP-50 and CF-70 are...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2020· Boston Scientific

Recalled Item: Stretch VL Ureteral Stent Set 6FX22- 30CM with .035 Sensor UPN:...

The Issue: An increase in the rate of complaints for difficulty or inability to track...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2020· Boston Scientific

Recalled Item: Percuflex Plus Ureteral Stent Set 6FX26CM with .038 Sensor UPN:...

The Issue: An increase in the rate of complaints for difficulty or inability to track...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2020· Boston Scientific

Recalled Item: Sensor Nitinol Wire with Hydrophilic Tip .035 3CM FLEX /150CM Recalled by...

The Issue: An increase in the rate of complaints for difficulty or inability to track...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2020· Boston Scientific

Recalled Item: Polaris Ultra Ureteral Stent Set 6FX24CM with .035 Sensor UPN: M006192132080...

The Issue: An increase in the rate of complaints for difficulty or inability to track...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2020· Boston Scientific

Recalled Item: Sensor Nitinol Wire with Hydrophilic Tip .0383CM FLEX ANG/150CM UPN:...

The Issue: An increase in the rate of complaints for difficulty or inability to track...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2020· Boston Scientific

Recalled Item: Percuflex Plus Ureteral Stent Set 7FX24CM with .035 Sensor UPN: Recalled by...

The Issue: An increase in the rate of complaints for difficulty or inability to track...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2020· Boston Scientific

Recalled Item: Stretch VL Ureteral Stent Set 4.8FX22-30CM with .035 Sensor UPN:...

The Issue: An increase in the rate of complaints for difficulty or inability to track...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing