The Recall Desk

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.

51901–51925 of 80980

  • ModerateFDA (Devices)·Z-2763-2016·2016-09-14

    Blackrock NeuroPort Biopotential Signal Processing System Recall for Labeling Error

    Blackrock Microsystems is recalling 81 Neural Signal Amplifiers because the device and patient cable are incorrectly labeled as Type CF Applied Parts.

    Product
    Neural Signal Amplifier. Part Numbers: 4208, 5703, 5749, 5748, 5747. Product Usage: The Blackrock NeuroPort Biopotential Signal Processing System supports recording, processing and display of biopotential signals from user supplied electrodes. Biopotential signals include…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2074-2016·2016-09-14

    Nature Made Hair Skin Nails Gummies Recalled for Microbial Count

    Pharmavite is recalling specific lots of Nature Made adult gummies Hair.Skin.Nails because they may exceed specifications for total viable plate count.

    Product
    Nature Made(R) adult gummies Hair.Skin.Nails, 150 count, UPC 0-31604-04132-8-1
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2109-2016·2016-09-14

    Inland Market Dungeness Crab Cake Recalled for Wood Contamination

    Inland Seafood, Inc. is recalling Inland Market Dungeness Crab Cake due to possible contamination with wood pieces.

    Product
    Inland Market, Dungeness Crab Cake, Net Wt. 5 lbs, Inland Market, 1667 Lewis Way, Stone Mountain, GA 30083, for Whole Foods Market
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-2102-2016·2016-09-14

    Inland Market Maine Lobster Spread Recalled for Wood Contamination

    Inland Seafood, Inc. is recalling Inland Market Maine Lobster Spread due to possible contamination with wood pieces.

    Product
    Inland Market, Premium, Maine Lobster Spread, Net Wt. 7 oz. (198 g.) and 16 oz. (454g), Inland Market, 1667 Lewis Way, Stone Mountain, GA 30083.
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-2764-2016·2016-09-14

    Blackrock NeuroPort Patient Cables Recalled for Incorrect Labeling

    Blackrock Microsystems is voluntarily recalling 120 Patient Cables because they are incorrectly labeled as Type CF Applied Parts.

    Product
    Patient Cable. Part Numbers: 4460, 6735. Sterile within Chipboard Boxes within corrugated cartons. Product Usage: The Blackrock NeuroPort Biopotential Signal Processing System supports recording, processing and display of biopotential signals from user supplied electrodes.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2110-2016·2016-09-14

    Inland Market Traditional Crab Cake Recalled for Wood Contamination

    Inland Seafood, Inc. is recalling Inland Market Traditional Crab Cake due to possible contamination with wood pieces.

    Product
    Inland Market, Traditional Crab Cake, Net Wt. 5 lbs, Inland Market, 1667 Lewis Way, Stone Mountain, GA 30083, for Whole Foods Market
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-2103-2016·2016-09-14

    Inland Seafood Recalls Cheese Spread for Possible Wood Contamination

    Inland Seafood, Inc. is recalling Original Seafood Cheese Spread for Publix due to possible contamination with wood pieces.

    Product
    Original Seafood Cheese Spread, Net Wt. 7 oz. (198 g.), for Publix
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Drugs)·D-1491-2016·2016-09-14

    Zydus Recalls Bromocriptine Mesylate Capsules Due to Stability Test Failures

    Zydus Pharmaceuticals is recalling 14,808 bottles of Bromocriptine Mesylate 5 mg capsules because stability samples failed impurity tests.

    Product
    BROMOCRIPTINE MESYLATE — BROMOCRIPTINE MESYLATE (BROMOCRIPTINE MESYLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2742-2016·2016-09-14

    Siemens ADVIA Centaur PSA Assay Recall for Clinical Interpretation Clarification

    Siemens Healthcare Diagnostics is recalling ADVIA Centaur PSA Assay kits to emphasize that PSA values must be interpreted according to current clinical guidelines for biochemical recurrence.

    Product
    ADVIA Centaur¿ PSA Assay; Cat No. 06574155/SMN 10310292 (100 test)/02676506/SMN 10310293 (500 test)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2073-2016·2016-09-14

    Nature Made Hair Skin Nails Gummies Recalled for Microbial Count

    Pharmavite is recalling specific lots of Nature Made adult gummies Hair.Skin.Nails because they may exceed specifications for total viable plate count.

    Product
    Nature Made(R) adult gummies Hair.Skin.Nails, 90 count, UPC 0-31604-04016-1
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2747-2016·2016-09-14

    Mentor Breast Tissue Expanders Recalled Due to Product Mix-Up

    Mentor Texas, LP. is recalling 65 units of MENTOR CPX4 breast tissue expanders because a 350cc unit was found in a carton intended for 450cc units.

    Product
    MENTOR 2" Tall Height TE With Sutures 350cc PN: 354-9312 The MENTOR CPX4 and CPX4 with Suture Tabs Breast Tissue Expanders are used for breast reconstruction following mastectomy and are intended for temporary subcutaneous or submuscular implantation and are not intended for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1481-2016·2016-09-14

    Amerisource Recalls Mispackaged Dextroamphetamine and Amphetamine Tablets

    Amerisource Health Services is recalling 221 cartons of mixed amphetamine tablets due to unit dose mispackaging, where blister cavities may contain more than one tablet.

    Product
    Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product) CII 5 mg, 30 UD Tablets (5 x 6), Rx, Packaged and Distributed by: American Health Packaging, Columbus…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1494-2016·2016-09-14

    Teva Recalls Argatroban Injection Due to Manufacturing Deviations

    Teva North America is voluntarily recalling 1,299 bags of Argatroban Injection due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    ARGATROBAN Injection in 0.9% Sodium Chloride 250 mg/250 mL (1 mg/mL) , Rx Only, Manufactured in Hungary for TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC# 0703-0020-31 (Single Use Bag), NDC # 0703-0020-32 (5 Single Use Bags in One Carton).
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2743-2016·2016-09-14

    Integra Recalls Achillon Suture System Due to Sterility Concerns

    Integra LifeSciences is recalling the Achillon Suture System because internal studies suggest the secondary package seal may not maintain intended sterility.

    Product
    Achillon Minimally Invasive Device for Achilles Tendon Rupture Treatment The Achillon Suture System is a single use, sterile device used to treat acute Achilles tendon ruptures. The Achillon Suture System is a mini-invasive procedure indicated to teat acute Achilles tendon…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2748-2016·2016-09-14

    Mentor CPX4 Breast Tissue Expanders Recalled for Product Mix-Up

    Mentor Texas, LP. is recalling 70 units of CPX4 breast tissue expanders because a 350cc product was found in a carton labeled for the 450cc version.

    Product
    MENTOR 2" Tall Height TE With Sutures 450cc PN: 354-9313 The MENTOR CPX4 and CPX4 with Suture Tabs Breast Tissue Expanders are used for breast reconstruction following mastectomy and are intended for temporary subcutaneous or submuscular implantation and are not intended for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2101-2016·2016-09-14

    Inland Market Blue Crab Spread Recalled for Wood Contamination

    Inland Seafood, Inc. is recalling Inland Market Premium Blue Crab Spread due to possible contamination with wood pieces.

    Product
    Inland Market, Premium Blue Crab Spread, Net Wt. 7 oz. (198 g.) and 16 oz. (454g), Inland Market, 1667 Lewis Way, Stone Mountain, GA 30083.
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-2077-2016·2016-09-14

    Nature Made Vitamin D Tablets Recalled for Yeast and Mold

    Pharmavite is recalling specific lots of Nature Made Vitamin D tablets because they may exceed specifications for yeast and mold.

    Product
    Nature Made(R) D3 1000IU, 125 count, UPC 0-31604-02793-3
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2075-2016·2016-09-14

    Nature Made Vitamin D tablets recalled for yeast and mold

    Pharmavite is recalling specific lots of Nature Made Vitamin D tablets because they may exceed specifications for yeast and mold.

    Product
    Nature Made(R) D3 1000IU, 100 count, UPC 0-31604-01870-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2076-2016·2016-09-14

    Nature Made Vitamin D Tablets Recalled for Potential Yeast and Mold

    Pharmavite is recalling specific lots of Nature Made Vitamin D tablets because they may exceed specifications for yeast and mold.

    Product
    Nature Made(R) D3 1000IU, 300 count, UPC 0-31604-02683-7
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2105-2016·2016-09-14

    Inland Seafood Recalls Alaskan Salmon Salad Due to Wood Contamination

    Inland Seafood, Inc. is recalling Alaskan Salmon Salad sold at Whole Foods Market due to possible contamination with wood pieces.

    Product
    Alaskan Salmon Salad, 12 x 8 oz. and 5 lb., for Whole Foods Market
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-2111-2016·2016-09-14

    Inland Market Maryland Crab Cake Recalled for Wood Contamination

    Inland Seafood, Inc. is recalling Inland Market Maryland Crab Cake due to possible contamination with wood pieces.

    Product
    Inland Market, Maryland Crab Cake, Net Wt. 5 lbs, Inland Market, 1667 Lewis Way, Stone Mountain, GA 30083, for Whole Foods Market
    Category
    Food
    Distribution
    11 states