The Recall Desk

State

South Carolina product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48351–48375 of 80970

  • HighFDA (Food)·F-2040-2017·2017-04-26

    Asher's Chocolate Peanut Butter Cups Recalled for Salmonella Risk

    Asher's Chocolate Co. is recalling specific lots of peanut butter cups due to potential Salmonella contamination. Consumers should check lot numbers and stop eating the product.

    Product
    Asher's Chocolate Co. Milk Chocolate (09611) Peanut Butter Cup 2.35 oz.; 24 pc./box.; Asher's Chocolate Co. Milk Chocolate (09618) Peanut Butter Cup Mini; 4 lb..; Asher's Chocolate Co. Milk Chocolate (11806) Peanut Butter Cup; 2.35 oz. 24/box.; Asher's Chocolate Co. Milk…
    Category
    Food
    Distribution
    41 states
  • HighFDA (Food)·F-2008-2017·2017-04-26

    Asher's Dark Chocolate Molasses Pops Recalled for Salmonella Risk

    Asher's Chocolate Co. is recalling Dark Chocolate Molasses Pops due to potential Salmonella contamination. Consumers should stop eating the product and return it to the store.

    Product
    Asher's Chocolate Co, Dark Chocolate (14814) FK Molasses Pop; Net Wt. 2 oz. (24/box).
    Category
    Food
    Distribution
    41 states
  • HighFDA (Devices)·Z-1849-2017·2017-04-26

    Smith & Nephew ACUFEX TRUNAV Retrograde Drill Recall for Blade Detachment Risk

    Smith & Nephew is recalling ACUFEX TRUNAV Retrograde Drills because the cutting blade may detach or the drill head may fracture during use.

    Product
    Smith & Nephew ACUFEX TRUNAV Retrograde Drill 11MM Product Number: 72204048 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a back bore socket in bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2058-2017·2017-04-26

    Asher's Chocolate Co. Milk Chocolate Cashew Praline Recalled for Salmonella Risk

    Asher's Chocolate Co. is recalling specific lots of Milk Chocolate Cashew Praline due to potential Salmonella contamination.

    Product
    Asher's Chocolate Co. Milk Chocolate (82016) Disney Cashew Praline; 15 - 3 oz. Piece box; Asher's Chocolate Co. Milk Chocolate (75008) Cashew Praline; 3 oz. (15/box)
    Category
    Food
    Distribution
    41 states
  • HighFDA (Food)·F-2036-2017·2017-04-26

    Asher's Peanut Butter Coated Mini Pretzels Recalled for Salmonella Risk

    Asher's Chocolate Co is recalling Peanut Butter Coated Mini Pretzels due to potential Salmonella contamination. Consumers should stop eating the product.

    Product
    Asher's Chocolate Co, Peanut Butter Coating (14775) FK Mini Pretzel DK String; Net Wt. 4 oz. (12/box);
    Category
    Food
    Distribution
    41 states
  • HighFDA (Food)·F-2079-2017·2017-04-26

    Asher's White Confectionery Coating Recalled for Potential Salmonella Contamination

    Asher's Chocolate Co is recalling White Confectionery Coating due to potential Salmonella contamination. Consumers should check their lot numbers and stop using the product.

    Product
    Asher's Chocolate Co, White Confectionery Coating (83426) Coconut Haystack, Net Weight 3 lb;
    Category
    Food
    Distribution
    41 states
  • HighFDA (Food)·F-2077-2017·2017-04-26

    Asher's Dark Chocolate Almond Paw Recalled for Salmonella Contamination Risk

    Asher's Chocolate Co is recalling Dark Chocolate Almond Paw products due to potential Salmonella contamination. Consumers should check for Lot # 000336473.

    Product
    Asher's Chocolate Co, Dark Chocolate (00401) Almond Paw, Net Wt. 4 lb
    Category
    Food
    Distribution
    41 states
  • ModerateFDA (Drugs)·D-0676-2017·2017-04-26

    Taro Recalls Nystatin and Triamcinolone Acetonide Cream for Stability Failures

    Taro Pharmaceuticals is recalling Nystatin and Triamcinolone Acetonide Cream because it failed content uniformity specifications during 18-month stability testing.

    Product
    NYSTATIN AND TRIAMCINOLONE ACETONIDE — NYSTATIN AND TRIAMCINOLONE ACETONIDE (NYSTATIN AND TRIAMCINOLONE ACETONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1837-2017·2017-04-26

    Alcon Recalls Patient Care Kits Due to Sterile Packaging Concerns

    Alcon is voluntarily removing 561,702 Patient Care Kits from the US market because the supplier reported potential sterile packaging compromise.

    Product
    Alcon Patient Care Kits Product Usage: A Patient Care Kit is an assemblage of single-use medical devices and accessories designed by medical professionals for specific procedures. The Patient Care kits are configured with customer-specific components
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1856-2017·2017-04-26

    Smith & Nephew Recalls D-RAD Orthopedic Screws Due to Incorrect Expiration Dates

    Smith & Nephew is recalling 100 units of D-RAD orthopedic screws because the expiration dates on the labels are incorrect and later than the actual expiration dates.

    Product
    D-RAD, 2.4MMX 20MM, S.T. CORTEX SCREW, QTY: (1), STERILE R, RES 74682420 Orthopedic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1852-2017·2017-04-26

    Verathon Recalls GVL 2 Stat Blades Packaged with Incorrect Size

    Verathon is recalling GVL 2 Stat blades (lot GC32825) because they were physically packaged with the incorrect size device, GVL 1 Stat blades.

    Product
    It is recommended for patients with weight/size between 4-22 lbs (1.8-10 kg). Part Number 0270-0429: GVL 2 Stat (box of 10 Stats). Part Number 0574-0027: GVL 2 Stat (single pouched Stat). Part Number 0270-0662: GlideScope AVL Video Baton 1-2 Kit (where one box of 10, part…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1828-2017·2017-04-26

    Merge Healthcare Recalls Eye Station and Eye Care PACS Software

    Merge Healthcare is recalling Eye Station and Eye Care PACS software because antivirus programs may permanently delete newly captured medical images.

    Product
    Merge Eye Station and Merge Eye Care PACS.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1857-2017·2017-04-26

    Smith & Nephew Recalls D-RAD Locking Screws Due to Incorrect Expiration Dates

    Smith & Nephew is recalling 197 units of D-RAD locking screws because the expiration dates on the labels are incorrect and later than the actual expiration dates.

    Product
    D-RAD, S.T. LOCKING SCREWS, T7, QTY: (1), STERILE R, in the following sizes: (a) 2.4MM X 10MM, RES 74692410 (b) 2.4MM X 12MM, RES 74692412 (c) 2.4MM X 16MM, RES 74692416 (d) 2.4MM X 22MM, RES 74692422 (e) 2.4MM X 24MM, RES 74692424
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1855-2017·2017-04-26

    Smith & Nephew Recalls D-RAD Locking Pegs Due to Incorrect Expiration Dates

    Smith & Nephew is recalling 19 units of D-RAD locking pegs because the expiration dates on the labels are incorrect and later than the actual dates.

    Product
    D-RAD, 1.8MM X 16MM, LOCKING PEG, QTY: (1), STERILE R, RES 74671816 Orthopedic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1854-2017·2017-04-26

    Smith & Nephew Recalls Peri-Loc VLP Self-Tapping Cortex Screws Due to Labeling Error

    Smith & Nephew is recalling specific Peri-Loc VLP self-tapping cortex screws because the expiration dates printed on the labels are incorrect and later than the actual dates.

    Product
    Peri-Loc(R) VLP 3.5 MM X 6 MM SELF-TAPPING CORTEX SCREW, QTY: (1), STERILE R, REF 71801306 Orthopedic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1835-2017·2017-04-26

    Ace Surgical Supply Recalls Incorrectly Packaged Dental Abutments

    Ace Surgical Supply Co., Inc. is recalling 87 INFINITY Internal Hex Healing Abutments because the incorrect device was packaged.

    Product
    INFINITY Internal Hex Healing Abutment, 4.5mm Platform, 4.7mm CW-3mm CH Straight; Product Code: 20145473 Product Usage: Non implantable dental abutment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0673-2017·2017-04-26

    Valeant Recalls CLENZIderm M.D. Acne Treatment Kits Due to Discoloration

    Valeant Pharmaceuticals is voluntarily recalling 5,647 units of CLENZIderm M.D. Acne Treatment Systems nationwide due to product discoloration.

    Product
    CLENZIderm M.D. Acne Treatment System, kit has 3 bottles a) Therapeutic Lotion (benzoyl peroxide 5% Acne Treatment) 47mL bottle, b) Daily Care Foaming Cleanser (Salicylic Acid 2% Acne Treatment) 118 mL bottle, c) Salicylic Acid 2% Acne Treatment 148mL, Valeant Pharmaceuticals…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0672-2017·2017-04-26

    Valeant Recalls CLENZIderm M.D. Pore Therapy Salicylic Acid Acne Treatment

    Valeant Pharmaceuticals is voluntarily recalling CLENZIderm M.D. Pore Therapy Salicylic Acid 2% Acne Treatment due to discoloration.

    Product
    CLENZIderm M.D. Pore Therapy Salicylic Acid 2% Acne Treatment 5 fl. oz. (148 mL), Valeant Pharmaceuticals North America LLC Distributed by OMP, Inc Long Beach, CA 90806 Made in USA. Product SKU 301876102042, NDC 0187-6102-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·17138·2017-04-25

    Zutano Recalls Infant Cozie Booties Due to Choking Hazard

    Zutano is recalling about 38,000 infant Cozie booties because the rubber grips on the bottom can detach and pose a choking hazard.

    Product
    Infant Cozie booties
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V273000·2017-04-25

    Ram ProMaster Recall for Incorrect Air Bag Labeling

    Chrysler is recalling 2014-2017 Ram ProMaster vehicles because labels incorrectly state they have frontal air bags. This mislabeling may increase injury risk in a crash.

    Product
    RAM — RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide