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. 2,579 recalls have been distributed to Arizona in the last 12 months.
Showing 28821–28840 of 52,339 recalls
Recalled Item: Respire Pink+ Hard/Soft Oral Sleep Apnea Device Recalled by Respire Medical...
The Issue: Potential for device breakage during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Respire Pink+ Hard Oral Sleep Apnea Device Recalled by Respire Medical Due...
The Issue: Potential for device breakage during use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ELAN 4 Air System is intended for high speed cutting Recalled by...
The Issue: The ELAN 4 Air System was released to the market place prior to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta ERGO++ Product Usage: ERGO is often used for stereotactic treatments....
The Issue: Incorrect DICOM mapping of the exported collimator or couch angles from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AERO IOL Injection System containing 10 Z28 Cartridges per box Recalled by...
The Issue: The recommended storage temperature on the label is incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electric Wheelchair bases: a) C300 b) C350 c) C400 d) C500 Recalled by...
The Issue: There is a potential failure of the top plate assembly, which is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II Recalled by...
The Issue: There is a potential failure of the top plate assembly, which is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Amia Automated Peritoneal Dialysis Set with Cassette Recalled by...
The Issue: The firm received increased customer complaints for Missing Red Line,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Berry Flavor Immune Support Dietary Supplement Effervescent Tablets 10...
The Issue: The label does not list "Sodium" in the ingredient statement.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Orange Flavor Immune Support Dietary Supplement Effervescent Tablets 10...
The Issue: The label does not list "Sodium" in the ingredient statement.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1113 Gravity Tube Set Pk/24 -SH Product Usage: The FMS Recalled by DePuy...
The Issue: Leakage of FMS gravity tub sets (281113) at the bulb and tube connection
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.via systems with SW VB20A Recalled by Siemens Medical Solutions USA,...
The Issue: A software update was released on August 22, 2017. Performing this software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Cage Recalled by Exactech, Inc. Due to Mislabeling
The Issue: Potentially mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Cage Recalled by Exactech, Inc. Due to Mislabeling
The Issue: Potentially mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile Mini C-arm system Part # 1000-0004. Intended to provide Recalled by...
The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile Mini C-arm system Part # 1000-0004-FD. Intended to provide Recalled...
The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile Mini C-arm system Part # 1000-0001. Intended to provide Recalled by...
The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile Mini C-arm system Part # 1000-0005. Intended to provide Recalled by...
The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vancomycin Hydrochloride for Injection Recalled by Pfizer Inc. Due to...
The Issue: Presence of Particulate Matter: glass particulate found in vial
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 30 mg over 9 hours...
The Issue: Defective Delivery System: Products no longer meet the release liner removal...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.