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. 2,723 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,723 in last 12 months

Showing 46214640 of 51,854 recalls

FoodAugust 28, 2024· Big Bottom Milk Company

Recalled Item: BIG BOTTOM MILK COMPANY Recalled by Big Bottom Milk Company Due to Required...

The Issue: Required pasteurization temperatures were not achieved.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 27, 2024· Safeguard US Operating LLC

Recalled Item: HAWK Advanced Hypothermia Management Set Recalled by Safeguard US Operating...

The Issue: Incorrect expiration date.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2024· Safeguard US Operating LLC

Recalled Item: Kits of Convenience containing 1 of the 2 Item Numbers: Recalled by...

The Issue: Incorrect expiration date.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 27, 2024· Safeguard US Operating LLC

Recalled Item: HAWK Warming Grid Recalled by Safeguard US Operating LLC Due to Incorrect...

The Issue: Incorrect expiration date.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2024· Nova Ortho-Med Inc

Recalled Item: Brand Name: NOVA ORTHO-MED INC. Product Name: MONARCH ROLLATOR BLUE Recalled...

The Issue: Firm identified a potential risk for a fall hazard. When the end user is...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2024· Qualigen Inc

Recalled Item: FastPack TSH Calibrator Kit Recalled by Qualigen Inc Due to Thyroid...

The Issue: Thyroid Stimulating Hormone (TSH) calibrator card has an incorrect barcode...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2024· Nova Ortho-Med Inc

Recalled Item: Brand Name: NOVA ORTHO-MED INC. Product Name: MONARCH ROLLATOR RED Recalled...

The Issue: Firm identified a potential risk for a fall hazard. When the end user is...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2024· Nova Ortho-Med Inc

Recalled Item: Brand Name: NOVA ORTHO-MED INC. Product Name: MONARCH ROLLATOR PURPLE...

The Issue: Firm identified a potential risk for a fall hazard. When the end user is...

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

Class II — Potential Health HazardOngoing
FoodAugust 26, 2024· Refresco Beverages US Inc

Recalled Item: a.) Great Value 8oz Apple Juice in 6pack Recalled by Beverages US Inc Due to...

The Issue: Products contains inorganic arsenic above action level set in guidance to...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2024· Rubicon Research Private Limited

Recalled Item: AcetaZOLAMIDE Tablets Recalled by Rubicon Research Private Limited Due to...

The Issue: Discoloration

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 23, 2024· Young Dental Manufacturing I, LLC

Recalled Item: BIOTROL PURIT Clean-It General Purpose Ultrasonic Cleaner Recalled by Young...

The Issue: The bulk product used in the recalling firm's repackaged finished product...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2024· Olympus Corporation of the Americas

Recalled Item: Olympus Endoscopic Flushing Pump Recalled by Olympus Corporation of the...

The Issue: During product testing, Olympus identified an intermittent loss of function...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2024· Stryker Spine

Recalled Item: AVS Anchor-C Cervical Cage System Instructions For Use (IFU)- eIFU Recalled...

The Issue: Labeling Correction: Instructions For Use (IFU)-Updated electronic Rev 5,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: System Code Name: 722282 Azurion 7 M20 722281 Azurion 5 Recalled by PHILIPS...

The Issue: Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2024· Kinova Inc

Recalled Item: KINOVA Jaco assistive robot. Model Numbers: PJ 0000 0001 Recalled by Kinova...

The Issue: Potential installation issue that could result in a fire hazard in the event...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 22, 2024· Healgen Scientific Llc

Recalled Item: Healgen Series Reagent strips for Urinalysis are composed of several...

The Issue: The reason for this recall is Healgen Scientific Ltd. has determined that...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: System Name: 722044 INTEGRIS Allura 15-12 (biplane) 722030 Integris CV...

The Issue: Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: System Name: 722059 Allura Xper FD20/15 OR Table 722058 Allura Recalled by...

The Issue: Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2024· Medtronic Navigation, Inc.

Recalled Item: StealthStation S8 App versions 1.3.0 and 1.3.2 Recalled by Medtronic...

The Issue: Due to two software anomalies that can occur within a spine procedure. Two...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: System Name: 708038 MultiDiagnost Eleva with Flat Detector 708037...

The Issue: Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or...

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

Class II — Potential Health HazardOngoing