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. 2,595 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,595 in last 12 months

Showing 2246122480 of 52,339 recalls

Medical DeviceJune 19, 2019· Seca

Recalled Item: Seca 402/403 Baby Scale Cart Recalled by Seca Due to It has been determined...

The Issue: It has been determined that the wheels on the baby scale cart can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Elekta, Inc.

Recalled Item: iGUIDE System with software build iGuide 2.2.0 Recalled by Elekta, Inc. Due...

The Issue: Potential for iGUIDE to incorrectly monitor the 3D position.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Pharmaceutical Innovations, Inc.

Recalled Item: ElectroMist product codes: 36-3310-04 - Product Usage: Electrode...

The Issue: Potential for failed stability antimicrobial effectiveness testing.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Pharmaceutical Innovations, Inc.

Recalled Item: ElectroMist product codes: 36-3310-60 - Product Usage: Electrode...

The Issue: Potential for failed stability antimicrobial effectiveness testing.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex Med 4" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2019· Andover Healthcare Inc.

Recalled Item: Sterile Co-Flex NL 4" - Product Usage: Single Use secondary Recalled by...

The Issue: Incomplete packaging seal of sterile product

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2019· CooperSurgical, Inc.

Recalled Item: LEEP Precision Integrated System 120V & LEEP Precision Generator Recalled by...

The Issue: The products' cut, coagulate, or blend function may not operate with the use...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2019· Ad-Tech Medical Instrument Corporation

Recalled Item: LSB Style Anchor Bolt. Labeled with the following parts: 13mm Recalled by...

The Issue: On June 12, 2019 Ad-Tech was made aware that on three different occasions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2019· Howmedica Osteonics Corp.

Recalled Item: Serrato 9.5mm X 90mm Polyaxial Screw Catalog Number 482619590 Serrato...

The Issue: Discrepant length; Lot B88751 90mm screws were manufactured with a 100mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2019· Ad-Tech Medical Instrument Corporation

Recalled Item: Dual-Sided Interhemispheric Recalled by Ad-Tech Medical Instrument...

The Issue: Supplemental information provided with devices indicates that the subdural...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2019· Ad-Tech Medical Instrument Corporation

Recalled Item: Skull Anchor Bolts Recalled by Ad-Tech Medical Instrument Corporation Due to...

The Issue: Supplemental information provided with devices may indicate that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2019· Ad-Tech Medical Instrument Corporation

Recalled Item: Depth Electrodes Recalled by Ad-Tech Medical Instrument Corporation Due to...

The Issue: Supplemental information provided with devices indicates that the subdural...

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

Class II — Potential Health HazardOngoing
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Dexamethasone Sodium Phosphate Preservative Free Sterile Solution for INJ...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Droperidol Injectable Sterile Solution Recalled by Premier Pharmacy Labs Inc...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Brilliant Blue Ophthalmic PF INJ Recalled by Premier Pharmacy Labs Inc Due...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Neostigmine Methylsulfate Recalled by Premier Pharmacy Labs Inc Due to Lack...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: SUCCINYLcholine Chloride Recalled by Premier Pharmacy Labs Inc Due to Lack...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: SUCCINYLcholine Chloride Recalled by Premier Pharmacy Labs Inc Due to Lack...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Isoproterenol HCL in D5W (Non Sterile to Sterile) Recalled by Premier...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2019· Premier Pharmacy Labs Inc

Recalled Item: Sodium Bicarbonate INJ 8.4% Recalled by Premier Pharmacy Labs Inc Due to...

The Issue: Lack of Assurance of Sterility: FDA inspection found insufficient...

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

Class II — Potential Health HazardOngoing
Refund