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. 2,582 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,582 in last 12 months

Showing 2636126380 of 52,339 recalls

Medical DeviceJuly 12, 2018· Medical Components, Inc dba MedComp

Recalled Item: Duo-Flow IJ Full Tray Recalled by Medical Components, Inc dba MedComp Due to...

The Issue: The suture wings have the potential to crack or break. Potential patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Medical Components, Inc dba MedComp

Recalled Item: DUO FLOW DOUBLE LUMEN CATHETER Recalled by Medical Components, Inc dba...

The Issue: The suture wings have the potential to crack or break. Potential patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Medical Components, Inc dba MedComp

Recalled Item: Duo-Flow XTP Straight Full Set Recalled by Medical Components, Inc dba...

The Issue: The suture wings have the potential to crack or break. Potential patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Medical Components, Inc dba MedComp

Recalled Item: DUO FLOW CUSTOM TRAYS Recalled by Medical Components, Inc dba MedComp Due to...

The Issue: The suture wings have the potential to crack or break. Potential patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Medical Components, Inc dba MedComp

Recalled Item: Duo-Flow Double Lumen Soft Tip CRRT/ABP Catheter Set Recalled by Medical...

The Issue: The suture wings have the potential to crack or break. Potential patient...

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

Class II — Potential Health HazardOngoing
DrugJuly 11, 2018· Renaissance Lakewood, LLC

Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to...

The Issue: Superpotent Drug: lots out of specification for elevated sodium chloride and...

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

Class III — Low RiskOngoing
Refund
DrugJuly 11, 2018· Renaissance Lakewood, LLC

Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to...

The Issue: Superpotent Drug and Failed Stability Specifications: lot out of...

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

Class III — Low RiskOngoing
Refund
DrugJuly 11, 2018· Renaissance Lakewood, LLC

Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to Failed...

The Issue: Failed Stability Specifications: lot out of specification for elevated water...

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

Class III — Low RiskOngoing
Refund
FoodJuly 11, 2018· Papa John's Salads & Produce, Inc.

Recalled Item: Superfood Salad Kit - 6.8 lbs. - sold to Kroger Recalled by Papa John's...

The Issue: It was discovered that a bulk salad kit was produced using the wrong...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products CREA Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides did not meet the current claims for Limit of Blank (LoB), Limit...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides failed to meet current claims for Limit of Blank (LoB), Limit of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides do not meet the maximum allowable interference (MAI) claims for...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides do not meet the maximum allowable interference (MAI) claims for...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2018· Spacelabs Healthcare, Ltd.

Recalled Item: Arkon Anesthesia Delivery System with Arkon Software Version 2.70 Recalled...

The Issue: Arkon Anesthesia Delivery System may go into a failed state (mechanical...

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

Class I — Serious Health HazardOngoing
DrugJuly 10, 2018· Valeant Pharmaceuticals North America LLC

Recalled Item: Diazepam Rectal Gel Recalled by Valeant Pharmaceuticals North America LLC...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Product distributed...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 10, 2018· Arrow International Inc

Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...

The Issue: The packaging may not be sealed. If the packaging is compromised in this...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2018· Arrow International Inc

Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...

The Issue: The packaging may not be sealed. If the packaging is compromised in this...

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

Class II — Potential Health HazardOngoing
DrugJuly 9, 2018· Mylan Pharmaceuticals Inc.

Recalled Item: Triamterene and Hydrochlorothiazide Tablets Recalled by Mylan...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 9, 2018· Sorin CRM SAS

Recalled Item: Sorin Platinium CRT-D 1741 DF-4 Recalled by Sorin CRM SAS Due to Hardware...

The Issue: Hardware configuration may lead to overconsumption, followed by loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2018· Merit Medical Systems, Inc.

Recalled Item: ChloraPrep With Tint Recalled by Merit Medical Systems, Inc. Due to A...

The Issue: A nonsterile bulk product designated for further processing in a tray was...

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

Class II — Potential Health HazardOngoing