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. 928 recalls have been distributed to South Carolina in the last 12 months.
Showing 46361–46380 of 51,854 recalls
Recalled Item: Amlodipine Besylate Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lamotrigine Tablets Recalled by Mylan Pharmaceuticals Inc. Due to CGMP...
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ifosfamide Injection 1g/20mL Recalled by AmeriSource Bergen Due to...
The Issue: Temperature abuse: Certain vials of Ifosfamide IV products were not at...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ifosfamide Injection 3g/60 mL Recalled by AmeriSource Bergen Due to...
The Issue: Temperature abuse: Certain vials of Ifosfamide IV products were not at...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Besylate and Benazepril HCl Capsules Recalled by Mylan...
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Besylate and Benazepril HCl Capsules Recalled by Mylan...
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ciprofloxacin Tablets Recalled by Mylan Pharmaceuticals Inc. Due to CGMP...
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MAQUET Getinge Group CARDIOHELP Base Unit .7999 .8012 Recalled by Maquet...
The Issue: It has come to the attention of MAQUET that in certain rare instances, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access 2 Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the Access 2 Immunoassay System because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roasted Salted Mixed Nuts w/ Peanuts Recalled by Dutch Valley Food...
The Issue: Roasted Salted Mixed Nuts with Peanuts were recalled for undeclared tree...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Honey Roasted Peanuts Recalled by Dutch Valley Food Development Inc. Due to...
The Issue: Honey Roasted Peanuts were recalled due to undeclared milk (lactose) and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Rotoprone therapy System is an advanced patient care system Recalled by...
The Issue: The lock pin can become stuck in the "in" position during the manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harvest Graft Delivery System Recalled by Harvest Technologies Corporation...
The Issue: Potential for leur connector to leak or have cracks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P21x/5-1 MHz transducer Recalled by SonoSite, Inc. Due to FUJIFILM SonoSite...
The Issue: FUJIFILM SonoSite Inc. remove P21x/5-1 Transducer because the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Artis zee / zeego Angiography System is designed as Recalled by Siemens...
The Issue: There is a potential issue on running Artis systems running software VC1x...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Loratadine 24 HR-OTC Recalled by Physicians Total Care, Inc. Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: Affected lot numbers may contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Risperdal CONSTA (risperiDONE) Recalled by Janssen Pharmaceuticals, Inc. Due...
The Issue: Non-Sterility: Janssen is recalling one lot of Risperdal CONSTA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VERIFY¿ Dual Species Self-Contained Biological Indicator Recalled by Steris...
The Issue: STERIS has identified that the population of the G. stearothermophilus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith Medical Recalled by Smiths Medical ASD, Inc. Due to Smiths Medical is...
The Issue: Smiths Medical is conducting a voluntary recall of PORT-A-CATH¿ and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ready to Use Thymo-Cide Recalled by Wexford Labs Inc Due to Expired active...
The Issue: Expired active ingredient was used in the manufacture of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.