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.

54076–54100 of 80980

HighFDA (Devices)·Z-1610-2016·2016-05-11
Applied Medical Recalls Wilson Penile Implantation System Retractor Frame
Applied Medical Technology Inc is recalling Wilson Penile Implantation System Retractor Frames due to a reported open pouch that breaches sterilization validation.
Product
Wilson Penile Implantation System Retractor Frame, Retractor Stays & Penile Elevation Strap, SINGLE USE ONLY Rx ONLY (USA) STERILE EO Do Not Resterilize Product Usage: Indicated to aid in tissue retraction during a surgical procedure.
Category
Medical Device
Distribution
28 states
HighNHTSA·16V286000·2016-05-11
Great Lakes Drywall Pup Trailers Recalled for Rear Impact Guard Defect
Great Lakes is recalling 1998-2016 Drywall Pup trailers because rear impact guards do not meet federal safety standards, increasing injury risk in crashes.
Product
GREAT LAKES — GREAT LAKES DRYWALL PUP
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·16157·2016-05-11
TwinGo Recalls Baby Carriers Due to Waist Buckle Breakage Hazard
TwinGo is recalling about 4,000 baby carriers because the waist buckle can break, posing a fall hazard to children. No injuries have been reported.
Product
Baby carriers
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1598-2016·2016-05-11
Siemens MAGNETOM MRI Systems Recalled Due to Magnetic Table Cover Hazard
Siemens is recalling eight MAGNETOM Aera/Skyra MRI systems because the patient table's docking station cover may contain a magnetic plate that attracts to the main magnet.
Product
MAGNETOM Aera/Skyra Systems, whole body magnetic resonance imaging systems, Model numbers 10432914, 10432915. Docking station top cover (part no# 10591430) of the removable patient table.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1611-2016·2016-05-11
Applied Medical Recalls Wilson Implantation System Due to Sterilization Breach
Applied Medical Technology Inc is recalling 1,100 units of the Wilson Implantation System after a complaint revealed an open pouch that breached sterilization validation.
Product
Wilson Implantation System Product Usage: Indicated to aid in tissue retraction during a surgical procedure.
Category
Medical Device
Distribution
28 states
HighFDA (Devices)·Z-1609-2016·2016-05-11
Applied Medical Technology Recalls Self-Retaining Retractor Frames Due to Sterilization Breach
Applied Medical Technology is recalling 3,754 units of TLC Self-Retaining Retractor Frames because a complaint reported an open pouch, which breaches sterilization validation.
Product
TLC¿ Self-Retaining Retractor Frames SINGLE USE ONLY Rx ONLY (USA) STERILE EO Do Not Resterilize. Product Usage: Indicated to aid in tissue retraction during a surgical procedure.
Category
Medical Device
Distribution
28 states
HighFDA (Devices)·Z-1608-2016·2016-05-11
Applied Medical Recalls TLC Self Retaining Retractor Systems Due to Sterilization Breach
Applied Medical Technology Inc is recalling 5,334 units of TLC Self Retaining Retractor Systems because a complaint reported an open pouch that breaches sterilization validation.
Product
TLC¿ Self Retaining Retractor System Contents 1-RETRACTOR FRAME 6-ELASTIC STAYS STERILE EO Rx ONLY Product Usage: Indicated to aid in tissue retraction during a surgical procedure.
Category
Medical Device
Distribution
28 states
HighFDA (Devices)·Z-1586-2016·2016-05-11
Ab Sciex Analyst MD Software Recall for Incorrect Diagnostic Results
Ab Sciex is recalling Analyst MD software versions 1.6.1 and 1.6.2 because it may display wrong quantitative results, potentially leading to incorrect patient diagnoses.
Product
Analyst¿ MD Version 1.6.1 and 1.6.2 Software used with the following instruments: API 3200MD" LC/MS/MS System, Instrument Part Number: 5024501; 3200MD QTRAP¿ LC/MS/MS System, Instrument Part Number: 5024500; Triple Quad" 4500MD LC/MS/MS System, Instrument Part Number: 5031257…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1601-2016·2016-05-11
Siemens Syngo Dynamics PACS Software Recall for Workflow Error
Siemens is recalling 84 units of Syngo Dynamics software due to a defect that may cause old measurements to be carried forward into new reports.
Product
Syngo Dynamics; Kinetdx Picture Archiving and Communications System
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V290000·2016-05-11
Chrysler Recalls Jeep Wrangler Vehicles Due to Air Bag Clockspring Defect
Chrysler is recalling 2007-2010 Jeep Wrangler vehicles because dust contamination in the clockspring assembly may prevent the driver's air bag from deploying.
Product
JEEP — JEEP WRANGLER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V289000·2016-05-11
Pacific Coachworks Recalls 2016 Rage'N Toy Haulers for Label Error
Pacific Coachworks is recalling 2016 Rage'N toy haulers because an incorrect Cargo Carrying Capacity value on the Federal Information label could lead to overloading.
Product
PACIFIC COACHWORKS — PACIFIC COACHWORKS RAGE'N
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·16158·2016-05-11
Bosch Small Angle Grinders Recalled for Overheating and Burn Risk
Robert Bosch Tool Corp. is recalling about 91,000 Bosch 1380 Slim small angle grinders because they can overheat, melt brush covers, and expose hot components, posing a burn risk.
Product
Bosch small angle grinders
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-1293-2016·2016-05-11
Emerald Cashew Packs Recalled for Potential Glass Fragments
Diamond Foods is recalling Emerald 100 Calorie Packs of Cashew Halves & Pieces due to the potential for small glass fragments in the product.
Product
Emerald 100 Calorie Packs of Cashew Halves & Pieces, roasted and salted. 7 pack/ 0.62 oz. each (17.5 g). Ingredients: Cashews, Vegetable Oil/Safflower, Sunflower and/or Canola Oil, Salt, Rosemary extract (to preserve freshness: Retail Carton UPC: 0 10300 33324 1; Inner…
Category
Food
Distribution
23 states
ModerateFDA (Food)·F-1166-2016·2016-05-11
Iowa Select Herbs Recalls Cyperus Leaf for Misbranding and Adulteration
Iowa Select Herbs LLC is recalling 1-gallon bottles of Alcohol-Free Cyperus Leaf because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Product
Iowa Select Herbs LLC, Alcohol-Free, Cyperus Leaf, www.iowaselectherbs.com, 1 gallon, Cedar Rapids, IA 52402
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1164-2016·2016-05-11
Iowa Select Herbs Cranberry Recalled for Misbranding and Adulteration
Iowa Select Herbs LLC is recalling 7.5 fl. oz. bottles of Cranberry because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Product
Iowa Select Herbs LLC, Cranberry, www.iowaselectherbs.com, 7.5 fl. Oz., Cedar Rapids, IA 52402
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1197-2016·2016-05-11
Iowa Select Herbs Recalls Momordica Leaf for Misbranding and Adulteration
Iowa Select Herbs LLC is recalling Momordica Leaf under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Product
Iowa Select Herbs LLC, Momordica Leaf, www.iowaselectherbs.com, 1 gallon, Cedar Rapids, IA 52402
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1216-2016·2016-05-11
Iowa Select Herbs Recalls Rhodiola Root for Misbranding and Adulteration
Iowa Select Herbs LLC is recalling Rhodiola Root products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Product
Iowa Select Herbs LLC, Rhodiola Root, www.iowaselectherbs.com, 1 gallon., Cedar Rapids, IA 52402
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1184-2016·2016-05-11
Iowa Select Herbs Hawthorn Berry Recalled for Misbranding and Adulteration
Iowa Select Herbs LLC is recalling Hawthorn Berry dietary supplements because they are misbranded, unapproved new drugs, and adulterated.
Product
Iowa Select Herbs LLC, Hawthorn Berry (Crateagus oxycanthus), www.iowaselectherbs.com, 7.5 fl. Oz., Cedar Rapids, IA 52402
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1233-2016·2016-05-11
Iowa Select Herbs Recalls Yohimbe Bark for Misbranding and Adulteration
Iowa Select Herbs LLC is recalling Yohimbe Bark products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Product
Iowa Select Herbs LLC, Yohimbe Bark (Pausinystalia Yohimbe), www.iowaselectherbs.com, (a) 2 fl. Oz., (b) 4 fl. Oz., (c) 1 gallon, Cedar Rapids, IA 52402
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1209-2016·2016-05-11
Iowa Select Herbs Recalls Propolis Supplement for Misbranding and Adulteration
Iowa Select Herbs LLC is recalling Propolis (Ligustrum lucidum) supplements because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Product
Iowa Select Herbs LLC, Propolis (Ligustrum lucidum), 4 fl. Oz., www.iowaselectherbs.com, Cedar Rapids, IA 52402
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1187-2016·2016-05-11
Iowa Select Herbs Recalls Jewel Weed for Misbranding and Adulteration
Iowa Select Herbs LLC is recalling Jewel Weed under a consent decree because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
Product
Iowa Select Herbs LLC, Jewel Weed, www.iowaselectherbs.com, 1 gallon, Cedar Rapids, IA 52402
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1196-2016·2016-05-11
Iowa Select Herbs Recalls Milk Thistle Seed for Misbranding and Adulteration
Iowa Select Herbs LLC is recalling Milk Thistle Seed products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
Product
Iowa Select Herbs LLC, Milk Thistle Seed (Carduus marianus), www.iowaselectherbs.com, (a) 4 fl. Oz., (b) 16 fl. Oz., (c) 32 fl. Oz., Cedar Rapids, IA 52402
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1590-2016·2016-05-11
Biosense Webster Recalls Pentaray Catheters for Labeling Clarification
Biosense Webster is recalling Pentaray NAV High-Density Mapping Catheters to clarify contraindication language regarding patients with prosthetic valves.
Product
Pentaray NAV High-Density Mapping Catheter, Catalog No. D128201, D128202, D128203, D128204, D128205, D128206 The Biosense Webster Pentaray NAV High-Density Mapping Catheter is intended for multiple electrode electrophysiological mapping of cardiac structures in the heart…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1597-2016·2016-05-11
Alcon Recalls INFINITI Ultrasound Packs Due to Tubing Leakage
Alcon Research is recalling INFINITI Ultrasound Packs because the irrigation line tubing may leak near the white luer.
Product
INFINITI Ultrasound Pack. Catalog Numbers: 8065751716, 8065751717, 8065751718, 8065751720, 8065751721, 8065751723. An ophthalmic microsurgical system indicated for phacoemulsification and removal of cataracts.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1593-2016·2016-05-11
Carestream Image Suite V3 Recalled for Incorrect Image Annotation
Carestream Health is recalling Image Suite V3 units due to a software error that displays incorrect left/right image annotations.
Product
CARESTREAM Image Suite V3: MINI-PACS/F IMG ST/CLASSIC: REF/Catalog # 1036490; MINI-PACS/F IMG ST/POC&VITA: REF/Catalog # 1036508; MINI-PACS/F IMG ST/CLASSIC/INDIA: REF/Catalog # 1036417; MINI-PACS/F IMG ST/ POC&VITA /INDIA: REF/Catalog # 1036425 -- Made in USA by: Carestream…
Category
Medical Device
Distribution
Distributed nationwide