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. 2,764 recalls have been distributed to Arizona in the last 12 months.
Showing 6741–6760 of 29,154 recalls
Recalled Item: DEVILBISS HEALTHCARE 1025 SERIES OXYGEN CONCENTRATOR Recalled by DeVilbiss...
The Issue: The instruction manual is being replaced with an updated version that is in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Anti-SARSCoV- 2 Total N Antibody...
The Issue: Incorrect Number of Calibrator Levels (2) Set for the VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DigitalDiagnost C50 -intended for use in generating radiographic...
The Issue: If the PM for the telescopic carriage is not performed annually as defined...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C50 1.1-intended for use in generating radiographic images...
The Issue: If the PM for the telescopic carriage is not performed annually as defined...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MectaLIF ANTERIOR - Lag Plate Flush H10 Recalled by Medacta Usa Inc Due to...
The Issue: There is a potential for breakage of the small screw used to affix the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQURE Software Versions 2.5.2 2.5.3 2.5.4 2.6.0 2.6.1 Recalled by Radiometer...
The Issue: Due to potential software issue that may result in patient mix-up information.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MectaLIF ANTERIOR - Lag Plate Flush H14 Recalled by Medacta Usa Inc Due to...
The Issue: There is a potential for breakage of the small screw used to affix the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Gastrointestinal (GI) Panel for FILMARRAY Systems Recalled by...
The Issue: Due to manufacturing issue, Gastrointestinal (GI) Panel may result in false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MectaLIF ANTERIOR - Antibackout Lag Cover Recalled by Medacta Usa Inc Due to...
The Issue: There is a potential for breakage of the small screw used to affix the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MectaLIF ANTERIOR - Lag Plate Flush H18 Recalled by Medacta Usa Inc Due to...
The Issue: There is a potential for breakage of the small screw used to affix the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MectaLIF ANTERIOR - Lag Plate Flush H12 Recalled by Medacta Usa Inc Due to...
The Issue: There is a potential for breakage of the small screw used to affix the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MectaLIF ANTERIOR - Lag Plate Flush H16 Recalled by Medacta Usa Inc Due to...
The Issue: There is a potential for breakage of the small screw used to affix the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Samsung GM85 Digital X-ray Imaging System-A Digital Diagnostic Mobile X-ray...
The Issue: Issue related to the operation of the arm latch within the column that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REX (Recovery Exercise X-Trainer) Pressure Therapy System- USER Manual....
The Issue: Error in the Introduction section of the user manual that indicates the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EARLYVUE VS30 VITAL SIGNS MONITOR Software Version A.00.02 and A.00.01...
The Issue: EarlyVue VS30 Vital Signs Monitor and EarlyVue VS30 Vitals monitor Missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EarlyVue VS30 Vitals monitor with Software Versions A.00.02 and A.00.01...
The Issue: EarlyVue VS30 Vital Signs Monitor and EarlyVue VS30 Vitals monitor Missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System Recalled by Maquet...
The Issue: Some batches of product were not sterilized to their minimum sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VASOVIEW HEMOPRO Recalled by Maquet Cardiovascular, LLC Due to Some batches...
The Issue: Some batches of product were not sterilized to their minimum sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System Recalled by Maquet...
The Issue: Some batches of product were not sterilized to their minimum sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90 R.1.0 Recalled by Philips North America Due to Philips has...
The Issue: Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.