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. 1,880 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
1,880 in last 12 months

Showing 2584125860 of 51,854 recalls

DrugAugust 3, 2018· Westminster Pharmaceuticals LLC

Recalled Item: Levothyroxine and Liothyronine (Thyroid Tablets Recalled by Westminster...

The Issue: Failed Content Uniformity Specifications: Product was manufactured using an...

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 3, 2018· Hostess Brands, LLC

Recalled Item: Hostess Brownies Cookies 'n Cr¿me packaged in the following ways: Recalled...

The Issue: The product ingredients statement declares egg ingredients, but the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 3, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Multix Fusion system is a radiographic system: Models: Multix Fusion...

The Issue: Steel cables inside the lifting column of the overhead tube, may rapture...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2018· Agfa Healthcare NV

Recalled Item: Enterprise Imaging Desktops Enterprise Imaging Desktops (Radiology...

The Issue: Adding an additional comparison study to the Clinical Side Bar in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2018· Zimmer Biomet, Inc.

Recalled Item: Biomet Sports Medii cine Juggerknot Long Flex Drill Bit with Recalled by...

The Issue: Expiration date incorrectly listed on the label

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2018· Elekta, Inc.

Recalled Item: MOSAIQ Oncology Information System Recalled by Elekta, Inc. Due to Order...

The Issue: Order Status Remains Approved When Should Indicate Complete.

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

Class II — Potential Health HazardOngoing
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Ipamorelin 3 mg Lyophilized 1 vial 1109 East Hallandale Beach Recalled by...

The Issue: Lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Human Chorionic Gonadotropin 6000 IU Vial Lyophilized 1109 East Hallandale...

The Issue: Lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Human Chorionic Gonadotropin 20000 IU Vial Lyophilized 1109 East Hallandale...

The Issue: Lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Methylcobalamin 10 mg vial Lyophilized 1109 East Hallandale Beach Blvd....

The Issue: Lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Human Chorionic Gonadotropin 5000 IU Vial Lyophilized 1109 East Hallandale...

The Issue: Lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Ipamorelin 9 mg vial Lyophilized 1109 East Hallandale Beach Blvd. Recalled...

The Issue: Lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Human Chorionic Gonadotropin 4000 IU Vial Lyophilized 1109 East Hallandale...

The Issue: Lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Human Chorionic Gonadotropin 2500 IU Vial Lyophilized 1109 East Hallandale...

The Issue: Lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2018· Pharmcore Inc.

Recalled Item: Human Chorionic Gonadotropin 11000 IU Vial Lyophilized 1109 East Hallandale...

The Issue: Lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 2, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium tablets Recalled by Dr. Reddy's Laboratories, Inc. Due...

The Issue: Failed Impurities/Degradation Specifications - OOS was observed for ATV...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 2, 2018· Acumedia Manufacturers, Inc.

Recalled Item: Palcam Agar Base Recalled by Acumedia Manufacturers, Inc. Due to Expiration...

The Issue: Expiration date on the label is incorrect. Correct expiration date was...

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

Class III — Low RiskOngoing
Medical DeviceAugust 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment...

The Issue: The implant only has one bolt in the sterile package but it should have had two.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2018· Zimmer Biomet, Inc.

Recalled Item: Vanguard 360 Revision Knee System 63x 10mm Universal Tibial Block Augment...

The Issue: The implant only has one bolt in the sterile package but it should have had two.

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

Class II — Potential Health HazardOngoing
DrugAugust 1, 2018· American Health Packaging

Recalled Item: Doxycycline Hyclate Tablets Recalled by American Health Packaging Due to...

The Issue: Failed Dissolution Specifications: Out of specification result for the...

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

Class II — Potential Health HazardOngoing
Refund