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. 2,717 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,717 in last 12 months

Showing 60416060 of 51,854 recalls

Medical DeviceApril 15, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation 4000 7-Drawer Auxiliary Tower Recalled by CareFusion...

The Issue: Potential fluid ingress of anesthesia station or med station may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2024· Covidien, LP

Recalled Item: Tri-Staple 2.0 Black Reinforced Intelligent Reload- Applications in...

The Issue: Potential damage to the cartridge can result in poor staple formation and/or...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis" MedStation ES 7-Drawer Auxiliary Tower Recalled by CareFusion 303,...

The Issue: Potential fluid ingress of anesthesia station or med station may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2024· Maquet Medical Systems USA

Recalled Item: CARDIOHELP-i System. Blood oxygenation and carbon dioxide removal system....

The Issue: The firm identified that the measured patient leakage current in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2024· Philips North America Llc

Recalled Item: Incisive CT - Computed Tomography X-Ray System intended to produce Recalled...

The Issue: Metal mounting box on the rotating scanner on rotor (heat change box)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2024· Philips North America Llc

Recalled Item: Incisive CT - Computed Tomography X-Ray System intended to produce Recalled...

The Issue: Metal mounting box on the rotating scanner on rotor (heat change box)...

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

Class II — Potential Health HazardOngoing
DrugApril 12, 2024· Dercher Enterprises, Inc., DBA Gordon Laboratories

Recalled Item: Gordofilm Wart Remover (salicylic acid 16.7% USP) packaged in 15 cc glass...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 12, 2024· Medartis Inc.

Recalled Item: APTUS 2.8 TriLock Screw 22mm Recalled by Medartis Inc. Due to Screw is 16mm...

The Issue: Screw is 16mm long instead of 22mm long.

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

Class II — Potential Health HazardOngoing
FoodApril 11, 2024· The James Skinner Co.

Recalled Item: Marketside Cinnamon Pecan Braid Recalled by The James Skinner Co. Due to...

The Issue: Product has incorrect back label that does not declare pecans are present in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 11, 2024· Securitas Healthcare LLC

Recalled Item: Arial mobile application Recalled by Securitas Healthcare LLC Due to The...

The Issue: The Arial Mobile Application utilizing Apple iOS 17.4 and iOS 17.5 is...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: FDR Visionary Suite - Intended to generate digital or conventional Recalled...

The Issue: Bolts on the CH-200 tube may rupture due to fatigue failure, causing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: Noblus AC Adapter used with the Noblus Ultrasound Imaging System Recalled by...

The Issue: AC adapters of Noblus can heat up, and cause smoke in the worst case, when...

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

Class II — Potential Health HazardOngoing
FoodApril 10, 2024· FEEL GOOD FOODS INC

Recalled Item: Cream Cheese Stuffed Plain Mini Bagels Recalled by FEEL GOOD FOODS INC Due...

The Issue: Contains undeclared gluten

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 10, 2024· FEEL GOOD FOODS INC

Recalled Item: Cream Cheese Stuffed Everything Mini Bagels Recalled by FEEL GOOD FOODS INC...

The Issue: Contains undeclared gluten

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 10, 2024· Imprimis NJOF, LLC

Recalled Item: Prednisolone Sodium Phosphate-Moxifloxacin-Bromfenac Sterile Ophthalmic...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 10, 2024· Imprimis NJOF, LLC

Recalled Item: Epinephrine-Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL Preservative-Free...

The Issue: Out of specification for assay

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 10, 2024· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Leica HistoCore PEGASUS Tissue Processor Recalled by LEICA BIOSYSTEMS...

The Issue: Poorly processed and/or damaged biopsy tissue specimens on the device...

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

Class II — Potential Health HazardOngoing
DrugApril 9, 2024· Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.

Recalled Item: Abilify (aripiprazole) Recalled by Second Tokushima Factory, Otsuka...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
DrugApril 9, 2024· Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.

Recalled Item: Abilify (aripiprazole) Recalled by Second Tokushima Factory, Otsuka...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund
DrugApril 9, 2024· Second Tokushima Factory, Otsuka Pharmaceutical Co., Ltd.

Recalled Item: Abilify (aripiprazole) Recalled by Second Tokushima Factory, Otsuka...

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskOngoing
Refund