Product Recalls in Kansas
Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,616 recalls have been distributed to Kansas in the last 12 months.
Showing 4541–4560 of 28,538 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: 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 CLUSTER54E- 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 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 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 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 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 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 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: 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: 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 scalpel handle kits labeled as: a) STERILE # 3 SCALPEL HANDLE...
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 STERILE #16 RUBBER BAND Recalled by MEDLINE INDUSTRIES, LP -...
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: MEDLINE M1S0179 STRL TAPE/PEN PACK Recalled by MEDLINE INDUSTRIES, LP -...
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 manual surgical kits labeled as: a) STERILE ALLIS TISS FCP 10"...
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.