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. 1,133 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
1,133 in last 12 months

Showing 881–900 of 51,854 recalls

Medical DeviceOctober 31, 2025· Stryker Corporation

Recalled Item: NICO Myriad Handpiece Product Number/Product Name: NN-8000 15x10 MHP...

The Issue: Tape used to secure components within packaging contains latex, despite...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue MP2. Product Number: M8102A. Recalled by Philips North America...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX550. Product Number: 866066. Recalled by...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Multi-Measurement Module X3. Product Number: 867030. Recalled by...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Aizu Olympus Co., Ltd.

Recalled Item: Olympus OER-Pro Recalled by Aizu Olympus Co., Ltd. Due to Inform existing...

The Issue: Inform existing affected device customers about pertinent Warnings/Cautions,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX400. Product Number: 866060. Recalled by...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Stryker Medical Division of Stryker Corporation

Recalled Item: Stryker MV3 bariatric bed Recalled by Stryker Medical Division of Stryker...

The Issue: Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX750. Product Number: 866471. Recalled by...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue MP5. Product Number: M8105A. Recalled by Philips North America...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue MP20. Product Number: M8001A. Recalled by Philips North America...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue MP60. Product Number: M8005A. Recalled by Philips North America...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX600. Product Number: 865242. Recalled by...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing
FoodOctober 30, 2025· Lotus Vaping Technologies, LLC

Recalled Item: Monarch Premium Kratom Bali Gold powder is packaged in seal Recalled by...

The Issue: Product has the potential to be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 30, 2025· Lotus Vaping Technologies, LLC

Recalled Item: Monarch Premium Kratom Red Bali powder is packaged in seal Recalled by Lotus...

The Issue: Product has the potential to be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 30, 2025· Lotus Vaping Technologies, LLC

Recalled Item: Monarch Premium Kratom White Elephant powder is packaged in seal Recalled by...

The Issue: Product has the potential to be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 30, 2025· Lotus Vaping Technologies, LLC

Recalled Item: Monarch Premium Kratom Green Maeng Da powder is packaged in Recalled by...

The Issue: Product has the potential to be contaminated with Salmonella

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 29, 2025· Otsuka ICU Medical LLC

Recalled Item: POTASSIUM CHLORIDE Inj. Recalled by Otsuka ICU Medical LLC Due to Labeling:...

The Issue: Labeling: Label Error on Declared Strength-The overwrap label may...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 29, 2025· Otsuka ICU Medical LLC

Recalled Item: POTASSIUM CHLORIDE Inj. Recalled by Otsuka ICU Medical LLC Due to Labeling:...

The Issue: Labeling: Label Error on Declared Strength-The overwrap label may...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 29, 2025· Medtronic, Inc.

Recalled Item: Aurora EV-ICD and Clinical EV-ICD Recalled by Medtronic, Inc. Due to There...

The Issue: There is a potential for delayed time to high-voltage (HV) therapy should a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2025· Philips North America Llc

Recalled Item: CT 5300 Recalled by Philips North America Llc Due to If the screws of tube...

The Issue: If the screws of tube heat exchanger on the rotating scanner are not...

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

Class II — Potential Health HazardOngoing