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. 2,743 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,743 in last 12 months

Showing 16211640 of 51,854 recalls

Medical DeviceAugust 13, 2025· CHANGE HEALTHCARE CANADA COMPANY

Recalled Item: Change Healthcare Radiology Solutions software version 14.2.2 Recalled by...

The Issue: Due to software issue, radiology reports may not be fully displayed when...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Brilliance iCT Recalled by...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. IQon Spectral CT Recalled by...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Big Bore RT Recalled by...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Ingenuity CT Family Brazil...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. CT 6000 Recalled by Philips...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Brilliance 16 Power Recalled...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Brilliance CT 40 Channel...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Ingenuity CT 728326 Recalled...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Ingenuity Core128 Recalled...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Brilliance iCT SP Recalled...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Beckman Coulter Inc.

Recalled Item: UniCel DxH 800 COULTER Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Hematology analyzers configured with HGB photometers may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Beckman Coulter Inc.

Recalled Item: UniCel DxH 900 COULTER Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Hematology analyzers configured with HGB photometers may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Beckman Coulter Inc.

Recalled Item: UniCel DxH 690T COULTER Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Hematology analyzers configured with HGB photometers may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Beckman Coulter Inc.

Recalled Item: UniCel DxH 600 COULTER Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Hematology analyzers configured with HGB photometers may result in...

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

Class II — Potential Health HazardOngoing
DrugAugust 12, 2025· VIONA PHARMACEUTICALS INC

Recalled Item: Tavaborole Topical Solution 5% Recalled by VIONA PHARMACEUTICALS INC Due to...

The Issue: Discoloration

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 12, 2025· Max Mobility LLC

Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...

The Issue: Due to a faulty electrical connection between the speed control Dial and the...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 12, 2025· Max Mobility LLC

Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...

The Issue: Due to a faulty electrical connection between the speed control Dial and the...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 12, 2025· Max Mobility LLC

Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...

The Issue: Due to a faulty electrical connection between the speed control Dial and the...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 12, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Pheno. Image-Intensified Flouroscopic X-Ray System. Recalled by...

The Issue: Limited system movements after startup .

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

Class II — Potential Health HazardOngoing