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. 1,122 recalls have been distributed to Arizona in the last 12 months.
Showing 8301–8320 of 29,154 recalls
Recalled Item: CYSTO-URETHRO-FIBERSCOPE CYSTOSCOPE Recalled by Karl Storz Endoscopy Due to...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11272VN 11272VNK Flexible Video Urethro Cystoscope Z18442US-BD (08/2018)...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11001RD1 11001RDK1 KARL STORZ Slim Nasopharyngolaryngoscope 96216006US V5.0...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11272VUE 11272VUEK Flexible Video Cysto-Urethroscope 96136031USCA V1.1...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11274BCU1 11274BCUK1 Flexible Cystoscope Z18449US-BD (08-2018) Recalled by...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11272V CMOS VIDEO-CYSTO-URETHROSCOPE REV 11272VA 11272VAK CMOS...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11278VSA 11278VSAK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA...
The Issue: Failure to achieve the expected six-log reduction in microorganisms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge 9100-Series Washer Disinfector models: 9120E Recalled by Getinge Usa...
The Issue: Inadequate documentation verifying whether device installation has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical H/S ELLIPTOSPHERE CATH 5 FR Set-For administering contrast...
The Issue: Incorrect bonding material used for assembly of the catheter, may fail,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus DISPOSABLE GRASPING FORCEPS Recalled by Olympus Corporation of the...
The Issue: Forceps do not comply with Olympus standards for the amount of force...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical H/S CATHETER SET FR 5 with Integated Stylet Model: Recalled...
The Issue: Incorrect bonding material used for assembly of the catheter, may fail,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical H/S ELLIPTOSPHERE CATH 5 Fr -For administering contrast...
The Issue: Incorrect bonding material used for assembly of the catheter, may fail,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with...
The Issue: The Implantable Neurostimulator Model may be susceptible to not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dragonfly OpStar Imaging Catheter Recalled by Abbott Vascular Due to There...
The Issue: There is a potential that the proximal marker may separate from the imaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evans Wedge Disposable Trials Recalled by restor3d Inc. Due to During...
The Issue: During re-work of disposable instruments to relabel for 4-year shelf-life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-Sterile Double Ended Trial Kit Recalled by restor3d Inc. Due to Product...
The Issue: Product labeled incorrectly. The lot was labeled with Small footprint when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percept PC BrainSense Implantable Neurostimulator (INS) Model B35200...
The Issue: The Implantable Neurostimulator (INS) cannot communicate with the clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare TDX SP2 Recalled by Invacare Corporation Due to The battery wiring...
The Issue: The battery wiring harness on affected wheelchairs may become disconnected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroMARK Breast Biopsy Marker Recalled by Devicor Medical Products Inc Due...
The Issue: Small patient labels do not match the primary device label. The primary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percept BrainSense Implantable Neurostimulator (INS) Recalled by Medtronic...
The Issue: The Implantable Neurostimulator (INS) cannot communicate with the clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.