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. 984 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
984 in last 12 months

Showing 31941–31960 of 51,854 recalls

DrugMarch 7, 2017· Legacy Pharmaceutical Packaging LLC

Recalled Item: ATENOLOL Tablets Recalled by Legacy Pharmaceutical Packaging LLC Due to...

The Issue: Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2017· Pfizer Inc

Recalled Item: Quillivant XR (methylphenidate HCl) for extended-release oral suspension...

The Issue: Failed Dissolution Specifications: Dissolution at 8 hour was out of...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 7, 2017· Ulrich Medical USA Inc

Recalled Item: uNion Cervical Plate System Product Usage: The uNion Cervical Plate Recalled...

The Issue: Surgical technique was revised to prevent static plate screws blocking...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2017· Philips Electronics North America Corporation

Recalled Item: Philips IntelliVue MX4O WLAN Patient Wearable Monitor Product: 865352...

The Issue: Philips lntelliVue MX4O WLAN Patient Wearable Monitor may not automatically...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.via Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software changes now available to address several issues

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.x Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software changes now available to address several issues

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

Class II — Potential Health HazardOngoing
DrugMarch 6, 2017· GSK Consumer Healthcare

Recalled Item: Sensodyne Repair & Protect Whitening Recalled by GSK Consumer Healthcare Due...

The Issue: Presence of Foreign Substance; low concentration of an additional flavoring...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 6, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: ATENOLOL Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to Presence...

The Issue: Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 6, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: RIVASTIGMINE Tartrate Capsules Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Cross-contamination with other products -Related Substances test for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 3, 2017· Covidien LLC

Recalled Item: Covidien Curity Eye Pad Oval Recalled by Covidien LLC Due to Product...

The Issue: Product sterility is compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Covidien LLC

Recalled Item: Covidien Kerlix Super Sponge Saline Dressing Recalled by Covidien LLC Due to...

The Issue: Product sterility is compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Covidien LLC

Recalled Item: Covidien Curity Sodium Chloride Dressing Recalled by Covidien LLC Due to...

The Issue: Product sterility is compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Verathon Inc

Recalled Item: It is recommended for patients with weight/size between 4-22 lbs Recalled by...

The Issue: Product labeled as GVL 2 Stat (blades), lot GC32825, was physically packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Cardiovascular Systems Inc

Recalled Item: ViperWire Advance Peripheral Guide Wire with Flex Tip Recalled by...

The Issue: Cardiovascular Systems, Inc. is recalling one lot of ViperWire Advance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista 500 Intelligent Lab System and Dimension Vista 1500 Recalled...

The Issue: Siemens Healthcare Diagnostics has confirmed that in isolated cases when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Covidien LLC

Recalled Item: Covidien Curity Wet Dressing 8 x 4 (20.3 cm x 10.2 cm) Recalled by...

The Issue: Product sterility is compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Covidien LLC

Recalled Item: Covidien Curity Eye Pad Item Code: 91650 The sterile eye Recalled by...

The Issue: Product sterility is compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Covidien LLC

Recalled Item: Covidien Curity Eye Pad Item Code: 03201 The sterile eye Recalled by...

The Issue: Product sterility is compromised due to breach of sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Merit Medical Systems, Inc.

Recalled Item: The PreludeSYNC Radial Compression Device is a sterile Recalled by Merit...

The Issue: Merit Medical Systems, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2017· Integra LifeSciences Corp.

Recalled Item: Panta Nail Recalled by Integra LifeSciences Corp. Due to Voluntary...

The Issue: Voluntary recall/Removal of Panta and Panta XI Nails because there may be...

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

Class II — Potential Health HazardOngoing