Product Recalls in South Carolina

Product recalls affecting South Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to South Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,044 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
1,044 in last 12 months

Showing 17781–17800 of 51,854 recalls

Medical DeviceDecember 8, 2020· Becton Dickinson & Co.

Recalled Item: BD Phoenix PMIC/ID-107: IVD is intended for the in vitro Recalled by Becton...

The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2020· Oto Med Inc

Recalled Item: Grace Medical *** SHEEHY BONE DUST COLLECTOR *** Recalled by Oto Med Inc Due...

The Issue: During internal Age Testing, holes were found in the sterile Tyvek pouches...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2020· Oto Med Inc

Recalled Item: Grace Medical *** spineX BONE DUST COLLECTOR *** Recalled by Oto Med Inc Due...

The Issue: During internal Age Testing, holes were found in the sterile Tyvek pouches...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2020· Carl Zeiss Meditec AG

Recalled Item: IOLMaster 700 Recalled by Carl Zeiss Meditec AG Due to When using software...

The Issue: When using software 1.90.2.09 or 1.90.8.06 and using modality worklist...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2020· Oto Med Inc

Recalled Item: Grace Medical *** COX BONE DUST COLLECTOR *** Recalled by Oto Med Inc Due to...

The Issue: During internal Age Testing, holes were found in the sterile Tyvek pouches...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 7, 2020· Hikma Pharmaceuticals USA Inc.

Recalled Item: Sodium Chloride Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...

The Issue: Failed pH Specifications: Out of Specification pH Test Results were found in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2020· AVKARE Inc.

Recalled Item: TraZODONE Hydrochloride Tablets USP 100 mg Recalled by AVKARE Inc. Due to...

The Issue: Product mix-up: Bottles of sildenafil and trazodone were inadvertently...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugDecember 7, 2020· AVKARE Inc.

Recalled Item: Sildenafil Tablets USP 100 mg Recalled by AVKARE Inc. Due to Product mix-up:...

The Issue: Product mix-up: Bottles of sildenafil and trazodone were inadvertently...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodDecember 5, 2020· George DeLallo Co. Inc. New Stanton Warehouse and Production

Recalled Item: Holiday Cookie Platter packaged in plastic container 20 OZ (1.25 Recalled by...

The Issue: Undeclared pecans due to mis-labeling

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 5, 2020· VISBY MEDICAL INC

Recalled Item: visby medical COVID-19 Test kit *** An in vitro diagnostic Recalled by VISBY...

The Issue: Two issues: 1) 5 Lots were found to have incorrect labeling on the outer box...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 3, 2020· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets Recalled by Zydus...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 3, 2020· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets 15 mg Recalled by...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 2, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: CoaguChek XS Prof (Professional) Meters- IVD professional healthcare...

The Issue: Possible Misinterpretation of Displayed Measuring Units from INR to %Quick...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH 930 Analyzer - In vitro diagnostic testing of Recalled by...

The Issue: Multiple issues in Software v1.23.2 and lower-may lead to the reporting of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1600 Analyzer - In vitro diagnostic testing of Recalled by...

The Issue: Multiple issues in Software v1.23.2 and lower-may lead to the reporting of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 7.5"x13" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 4.5"x11" Heat Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temperature Tubing 6"x100'. One roll per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 6"x10" Heat Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2020· Steris Corporation

Recalled Item: Vis-U-All High Temp 4"x11" Self Seal Pouch 200 pouches per box Recalled by...

The Issue: Purple ink located on the outside label of Vis-U-All Pouches may migrate (...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing