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. 1,024 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
1,024 in last 12 months

Showing 19101–19120 of 51,854 recalls

DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Formula 82M (Minoxidil 5%/Tretinoin 0.01%/Fluocinolone acetonide 0.01%)...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Progesterone 150 mg Troche Recalled by MasterPharm LLC Due to Lack of...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· AAA Cosmetica, SA de CV

Recalled Item: bio aaa Advance Hand Sanitizer Ethyl Alcohol 70% Recalled by AAA Cosmetica,...

The Issue: Chemical Contamination: Product contains methanol.

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Finasteride Plus 1.25mg Capsule Recalled by MasterPharm LLC Due to Lack of...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Progesterone 50 mg Modified Release Capsule Recalled by MasterPharm LLC Due...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· AAA Cosmetica, SA de CV

Recalled Item: bio aaa Advance Hand Sanitizer Ethyl Alcohol 70% Recalled by AAA Cosmetica,...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Progesterone 200 mg Troche Recalled by MasterPharm LLC Due to Lack of...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Progesterone Modified Release 200 mg Capsule Recalled by MasterPharm LLC Due...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 1, 2020· Spartan Chemical Co Inc

Recalled Item: Lemon Blossom Hand Sanitizer (benzalkonium chloride 0.1% - antimicrobial)...

The Issue: Microbial contamination of non-sterile products: positive microbial...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 1, 2020· ICU Medical, Inc.

Recalled Item: 6' (15 cm) Appx 0.09 ml Recalled by ICU Medical, Inc. Due to Incorrect...

The Issue: Incorrect filter assemblies in IV administration set.

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

Class II — Potential Health HazardOngoing
DrugJuly 1, 2020· Preferred Pharmaceuticals, Inc.

Recalled Item: Lidothol Patch Recalled by Preferred Pharmaceuticals, Inc. Due to CGMP...

The Issue: CGMP Deviations: Contract Manufacturing Organization (CMO) misplaced/lost...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 30, 2020· Hill-Rom, Inc.

Recalled Item: Centrella Smart+ Bed Recalled by Hill-Rom, Inc. Due to Affected beds may...

The Issue: Affected beds may have screws installed that do not meet material tensile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2020· CareFusion 303, Inc.

Recalled Item: Alaris EtCO2 Module Model 8300 Recalled by CareFusion 303, Inc. Due to...

The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 30, 2020· Hill-Rom, Inc.

Recalled Item: Progressa Bed Recalled by Hill-Rom, Inc. Due to Affected beds may have...

The Issue: Affected beds may have screws installed that do not meet material tensile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2020· CareFusion 303, Inc.

Recalled Item: Alaris System PC Unit Model 8000 Recalled by CareFusion 303, Inc. Due to...

The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 30, 2020· CareFusion 303, Inc.

Recalled Item: Alaris System PC Unit Model 8000 modular infusion pump and monitoring system...

The Issue: If one or more screws or washers are loose or missing causing the battery...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 30, 2020· TELEFLEX MEDICAL INC

Recalled Item: Pleur-Evac Adult-Ped Wet Recalled by TELEFLEX MEDICAL INC Due to Potential...

The Issue: Potential for sterile packaging to be compromised¿

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2020· CareFusion 303, Inc.

Recalled Item: Alaris System PC Unit Model 8015 Recalled by CareFusion 303, Inc. Due to...

The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 30, 2020· Siemens Healthcare Diagnostics, Inc.

Recalled Item: DCA Vantage Handheld Barcode Scanner - Zebra Model - Model Recalled by...

The Issue: If DCA Vantage Analyzer is configured to run Code 39 with check digit, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2020· CareFusion 303, Inc.

Recalled Item: Alaris PCA Module Model 8120 - Product Usage: is intended Recalled by...

The Issue: LED display, which provides infusion or patient monitoring values, on the...

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

Class II — Potential Health HazardOngoing