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.
Showing 6261–6280 of 51,854 recalls
Recalled Item: Medline medical procedure kits labeled as follows: a) C-SECTION CDS Recalled...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits labeled as follows: a) MAJOR BREAST Recalled...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits labeled as follows: a) ARTHROSCOPY Recalled...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 48" Lead Wires Recalled by EBI, LLC Due to Damage to the lead wire sheath...
The Issue: Damage to the lead wire sheath (black cable) component and causing exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet SpinalPak Non-invasive Spine Fusion Stimulator System- Indicated for...
The Issue: Damage to the lead wire sheath (black cable) component and causing exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Redux Electrolyte Creme Recalled by Parker Laboratories, Inc. Due to Product...
The Issue: Product demonstrates low viscosity.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Patient Information Center (PIC) iX Uninterruptable Power Supply...
The Issue: Possible failure of Uninterruptable Power Supply (UPS) devices supporting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20" Lead Wires Recalled by EBI, LLC Due to Damage to the lead wire sheath...
The Issue: Damage to the lead wire sheath (black cable) component and causing exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet OrthoPak Non-invasive Bone Growth Stimulator System-Indicated for the...
The Issue: Damage to the lead wire sheath (black cable) component and causing exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amy's Kitchen Enchilada Verde Whole Meal 10 oz. 12 pk Item # 000085 Recalled...
The Issue: L. mono contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vancomycin Hydrochloride for Oral Solution Recalled by Amneal...
The Issue: Superpotent Drug: Due to overfilling of drug powder
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rifampin Capsules USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VCF Vaginal Contraceptive Film (nonoxynol-9 Recalled by Apothecus...
The Issue: cGMP Diviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AW-S025 NEO SONARMED SENSOR 2.5MM. Used in conjunction with SonarMed...
The Issue: The failure to detect the partial obstruction in a 2.5mm sensor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AW-S030 NEO SONARMED SENSOR 3.0MM. Used in conjunction with SonarMed...
The Issue: The failure to detect the partial obstruction in a 2.5mm sensor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AW-S035 NEO SONARMED SENSOR 3.5MM. Used in conjunction with SonarMed...
The Issue: The failure to detect the partial obstruction in a 2.5mm sensor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Artis Models: Interventional Fluoroscopic X-Ray Systems-Models:...
The Issue: Coolant level in the cooling circuit drops below a certain level, this may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 24K Premium Lense Recalled by Ontact Inc Due to Contact lenses recalled due...
The Issue: Contact lenses recalled due to potential bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Spectrum IQ Infusion Pump Recalled by Baxter Healthcare Corporation...
The Issue: One device was improperly performed testing prior to release from a Service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZPLP(Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate...
The Issue: Thread form issue for the locking holes in that the locking screws may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.