Product Recalls in Nevada
Product recalls affecting Nevada — including food, drugs, consumer products, medical devices, and vehicles distributed to Nevada. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,104 recalls have been distributed to Nevada in the last 12 months.
Showing 4541–4560 of 28,334 recalls
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 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 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: 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: 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: 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: Centurion Clamp kits labeled as: a) STERILE BACKHAUS TOWEL CLAMP (BTC173)...
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 Hemostat kits labeled as: a) STERILE CURV KELLY HEMOSTAT Recalled...
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 #5 LARYNGEAL MIRROR(505709) 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.
Recalled Item: Centurion STERILE BLOOD COLLECTION TUBE 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 STERILE COTTON DENTAL ROLLS 6/PK Recalled by MEDLINE INDUSTRIES,...
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: 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.
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.
Recalled Item: Centurion FCP MAGILL CATH 7.5 IN PED (67575) Recalled by MEDLINE INDUSTRIES,...
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 4-1/2" S/S Recalled by...
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: RayStation Software Version Numbers version numbers 8B Recalled by RAYSEARCH...
The Issue: A use error that has occurred with RayStation/RayPlan, where material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion Forcep kits labeled as: a) STERILE F/P SPLINTER FORCEP (SF6141)...
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.