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. 2,778 recalls have been distributed to Arizona in the last 12 months.
Showing 4581–4600 of 29,154 recalls
Recalled Item: Karl Storz SE & CO. KG Recalled by Karl Storz Endoscopy Due to Inadequate...
The Issue: Inadequate reprocessing validation evidence
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Performance Verifier II Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: The issue was mismatched diluent lots assembled into VITRO Chemistry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Performance Verifier I Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: The issue was mismatched diluent lots assembled into VITRO Chemistry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O.T.D - Optimum Traction Device - Street Orange. Single use traction splint....
The Issue: Failure of adhesive to secure the pole insert.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII HEMI CLUSTER52E-Indicated for use in primary and revision patients...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII PSL CLUSTER64H- Indicated for use in primary and revision Recalled...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII HEMI CLUSTER50D- Indicated for use in primary and revision...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII PSL CLUSTER50D- Indicated for use in primary and revision Recalled...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII PSL CLUSTER48D- Indicated for use in primary and revision Recalled...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII HEMI CLUSTER66H- Indicated for use in primary and revision...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII PSL CLUSTER58F-Indicated for use in primary and revision patients...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII HEMI CLUSTER58F- Indicated for use in primary and revision...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII HEMI CLUSTER44B- Indicated for use in primary and revision...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII PSL CLUSTER52E- Indicated for use in primary and revision Recalled...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII HEMI CLUSTER48D-indicated for use in primary and revision patients...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Sub-G Endotracheal Tube with Subglottic Suctioning: (1) Recalled by...
The Issue: Complaints have been received that the device inflation tube detached and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaviNetics Skull Anchor Key and Drill Kit Recalled by Navinetics Inc Due to...
The Issue: Defective Skull Anchor Key. After attachment of the single use Skull Anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Pressure Unit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: The firm provided a set of specifications for the device, but some units of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion Manual surgical kits labeled as: a) 15ML SAMPLING TUBE WITH CAP...
The Issue: Product may have a weak seal which may result in a breach of sterility of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion DISP.UMBILICAL CORD CLAMP CUTTER(CTR300) Recalled by MEDLINE...
The Issue: Product may have a weak seal which may result in a breach of sterility of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.