State

South Carolina product recalls

73,827 recalls have nationwide distribution and so reach South Carolina. 7,153 additional recalls listed South Carolina specifically in their distribution scope.

What the numbers show

Total: 7,153
Critical: 1,275
Severe: 2,170
Most recent: 2026-11-04

Of the 7,153 recalls naming South Carolina we have scored against our rubric, 1,275 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,170 (30%) are Severe.

Which agencies issued them

These figures cover only the 7,153 recalls whose distribution notice names South Carolina specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52801–52825 of 80980

CriticalFDA (Devices)·Z-1887-2016·2016-07-20
Heartware Ventricular Assist System Battery Recall for Premature Depletion
Heartware, Inc. is recalling 18,631 HeartWare Ventricular Assist System batteries due to premature depletion. The recall covers devices distributed nationwide in the US.
Product
HeartWare Ventricular Assist System: HeartWare Battery, Lithium Ion, 14.8 V, Rx only. Catalog 1650 (US) and 1650, 1650-DE and A00035 (OUS) Product Usage: Used as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage left…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1646-2016·2016-07-20
Dr. Praeger's California Veggie Burgers Recalled for Listeria Risk
Dr. Praeger's Sensible Foods is voluntarily recalling California Veggie Burgers because they may be contaminated with Listeria monocytogenes.
Product
Dr. Praeger's California Veggie Burgers, 26 x 10 oz./box, Best if used by: May-18-2018, UPC 0 80868 00010, Dr. Praeger's Sensible Foods, Elmwood Park, NJ 07407
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1335-2016·2016-07-20
Pharmakon Recalls Cefazolin Syringes Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling Cefazolin 1GM syringes because the company cannot ensure the product is sterile.
Product
Cefazolin 1GM in Sterile Water, 10 ml BD syringe, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0960-72
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1302-2016·2016-07-20
Pharmakon Recalls Magnesium Sulfate Injection Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 10 bags of Magnesium Sulfate 1GM in 0.9% Sodium Chloride due to a lack of assurance of sterility.
Product
Magnesium Sulfate 1GM Added to 0.9% Sodium Chloride, 50 mL bag, Rx only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0803-41
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1172-2016·2016-07-20
Medaus Recalls B-Complex 50 Vials Due to Sterility Concerns
Medaus, Inc. is recalling B-Complex 50 in NaCl 0.9% vials because the company cannot assure the sterility of the product.
Product
B-COMPLEX 50 IN NACL 0.9% (PF) B1-50MG, B2-5-PO4-5MG, B3-50MG, B5-50MG, B6-50MG/ML, 2ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1343-2016·2016-07-20
Pharmakon Recalls Bupivacaine Bags Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 70 units of Bupivacaine HCI 0.25% bags because the company cannot assure the products are sterile.
Product
Bupivacaine HCI 0.25% in 0.9% Sodium Chloride, 500 mL Intravia bag, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0994-03
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1652-2016·2016-07-20
Dr. Praeger's Recalls Black Bean Veggie Burgers Due to Listeria Risk
Dr. Praeger's Sensible Foods is voluntarily recalling specific lots of Black Bean Veggie Burgers because they may be contaminated with Listeria monocytogenes.
Product
Dr. Praeger's Black Bean Veggie Burger, 12 x 10 oz. (283 g)/box, Best if used by: May-12-2018, UPC 0 80868 06019 4, Dr. Praeger's Sensible Foods, Elmwood Park, NJ 07407
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1199-2016·2016-07-20
Medaus Recalls L-Phenylalanine Vials Due to Sterility Concerns
Medaus, Inc. is recalling specific lots of L-Phenylalanine 15mg/mL vials because the FDA cannot assure the product is sterile.
Product
L-PHENYLALANINE 15MG/ML (PF), 50ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1631-2016·2016-07-20
Dr. Praeger's Organic Harvest Veggie Burgers Recalled for Listeria Risk
Dr. Praeger's is voluntarily recalling Organic Harvest Veggie Burgers because they may be contaminated with Listeria monocytogenes.
Product
Dr. Praeger's Purely Sensible Foods Organic Harvest Veggie Burgers, 10 x 48 oz (1.36kg), Best if used by: May 16, 2017, UPC 0 8086830110 5, Dr. Praeger's Sensible Foods, Elmwood Park, NJ 07407
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2142-2016·2016-07-20
Hospira LifeCare Pump Model 4200 PCA Infuser Recalled for Occlusion Detection Failure
Hospira is recalling 6,268 LifeCare Pump Model 4200 PCA Infusers because they may fail to detect distal occlusions, a defect that caused one serious injury.
Product
The LifeCare Pump Model 4200 PCA Infuser makes possible the practical implementation of patient-controlled analgesia. The health care professional sets the prescribed dose, rates, and limits for the drug to be infused. The infuser can be set to operate in one of three modes: PCA…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1213-2016·2016-07-20
Medaus Recalls Manganese Sulfate Vials Due to Sterility Concerns
Medaus, Inc. is recalling Manganese Sulfate vials because the company cannot guarantee the product is sterile. The recall covers vials distributed in the U.S., Japan, and New Zealand.
Product
MANGANESE SO4 0.1MG/ML (PF), In a) 2MLVials and b) 10ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1328-2016·2016-07-20
Pharmakon Recalls Morphine Sulfate Syringes Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 340 units of Morphine Sulfate syringes due to a lack of assurance of sterility. The affected products were distributed nationwide and to specific VA/DOD locations.
Product
Morphine Sulfate 5mg/mL in 0.9% Sodium Chloride 25 mL fill in a 30 mL BD Syringe, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0935-67
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1315-2016·2016-07-20
Pharmakon Recalls Morphine Sulfate Bags Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 215 bags of Morphine Sulfate in Dextrose due to a lack of assurance of sterility. The affected products were distributed nationwide and to specific VA/DOD facilities.
Product
Morphine Sulfate 1 mg/mL in 5% Dextrose, 250 mL lntravia bag, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0875-02
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1169-2016·2016-07-20
Medaus Recalls B-Complex Vials Due to Sterility Assurance Concerns
Medaus, Inc. is recalling B-Complex (Lieberman) in NaCl 0.9% (PF) 2 mL vials due to a lack of assurance of sterility. The product was distributed in the U.S., Japan, and New Zealand.
Product
B-COMPLEX (LIEBERMAN) IN NACL 0.9% (PF), B1-12.5MG, B2-5-PO4-10MG, B3-12.5MG, B5-12.5MG, B6-12.5MG/ML, 2ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1257-2016·2016-07-20
Pharmakon Recalls Bupivacaine Injection Bags Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 130 bags of Bupivacaine 1mg/mL injection due to a lack of assurance of sterility. The product was distributed nationwide and to specific VA/DOD facilities.
Product
Bupivacaine 1mg/mL injection in 0.9% Sodium Chloride 250 mL bag, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0019-02
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1174-2016·2016-07-20
Medaus Recalls B-Complex Vials Due to Sterility Concerns
Medaus, Inc. is recalling specific lots of B-Complex with Cyanocobalamin vials because the company cannot ensure the product is sterile.
Product
B-COMPLEX W/CYANO B12 W/PRES., (BENZYL ETOH 2%), B1-100MG, B2-5-PO4-2MG, B3-50MG, B5-2MG, B6-2MG, CYANO B12 1MG/ML, In a) 2ML Vials, b) 5MLVials, c) 10ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1167-2016·2016-07-20
Medaus Recalls B-Complex #3 Vials Due to Sterility Concerns
Medaus, Inc. is recalling B-Complex #3 vials because the company cannot ensure the product is sterile. The recall covers vials distributed in the U.S., Japan, and New Zealand.
Product
B-COMPLEX #3 (PF), B1-100MG, B2-2-PO4-2MG, B3-100MG, B5-2MG, B6-2MG/ML, 2ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·16V545000·2016-07-20
Chrysler Recalls 2015-2016 Jeep Renegade for Trailer Hitch Fastener Defect
Chrysler is recalling 2015-2016 Jeep Renegade vehicles with factory trailer hitches because the assembly may be attached with too few fasteners, increasing crash risk.
Product
JEEP — JEEP RENEGADE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1243-2016·2016-07-20
Medaus Recalls Testosterone Cypionate Vials Due to Sterility Concerns
Medaus, Inc. is recalling specific lots of Testosterone Cypionate vials because the company cannot guarantee the product is sterile.
Product
TESTOSTERONE CYP 20 MG/ML W/PRES (BENZYL ETOH 2%), In a) 1ML Vials and b) 3ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1268-2016·2016-07-20
Pharmakon Recalls Adenosine Injection Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 12 units of Adenosine 1mg/ml injection due to a lack of assurance of sterility. The product was distributed nationwide and to specific VA/DOD facilities.
Product
Adenosine 1mg/ml (PF) in 0.9% Sodium Chloride (Total 90 mg/90 ml in 100 mL PAB Container); Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC # 45183-0146-47
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1341-2016·2016-07-20
Pharmakon Recalls Midazolam HCl Bags Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 10 bags of Midazolam HCl 1mg/mL due to a lack of assurance of sterility. The products were distributed nationwide and to specific VA/DOD facilities.
Product
Midazolam HCl 1mg/mL in 0.9% Sodium Chloride, 50 mL Intravia bag, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0989-41
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1225-2016·2016-07-20
Medaus Recalls M.I.C 25/50/50 Vials Due to Sterility Concerns
Medaus, Inc. is recalling M.I.C 25/50/50 vials because the product lacks assurance of sterility. The recall affects 2,000 mL in vials distributed in the U.S., Japan, and New Zealand.
Product
M.I.C 25/50/50 W/METHYL B12 1MG/PYRIDOXAL 50MG/ML (PF), 1ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1183-2016·2016-07-20
Medaus Recalls Estradiolval and Testosterone Vials Due to Sterility Concerns
Medaus, Inc. is recalling Estradiolval and testosterone vials because the company cannot ensure the product is sterile.
Product
ESTRADIOLVAL 3MG/TEST CYP 35MG/ TEST PROP 35MG/ML W/PRES. (BENZYL ETOH 2%), 3ML Vials, MEDAUS PHARMACY
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1282-2016·2016-07-20
Pharmakon Recalls Magnesium Sulfate Bags Due to Sterility Concerns
Pharmakon Pharmaceuticals is recalling 72 bags of Magnesium Sulfate in Lactated Ringers due to a lack of assurance of sterility. The products were distributed nationwide and to specific VA/DOD facilities.
Product
Magnesium Sulfate 50 GM in Lactated Ringers 500 mL bag; Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0407-03
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1348-2016·2016-07-20
Murray International Recalls Unapproved Sciatica Pills Marketed as Supplements
Murray International Trading Co. is recalling 144 bottles of Sciatica Pills because they are marketed as dietary supplements but contain drug claims, making them unapproved drugs.
Product
SCIATICA PILLS, packaged in 120-count bottles within a box, Made in the Peoples Republic of China, remaining labeling contains Chinese characters.
Category
Drug
Distribution
Distributed nationwide