State

South Carolina product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

57126–57150 of 80986

SevereFDA (Devices)·Z-0111-2016·2015-10-14
DePuy Orthopaedics Recalls Specialist 2 Intramedullary Rod Instruments Due to Fracture Complaints
DePuy Orthopaedics is voluntarily recalling select lots of the Specialist 2 Intramedullary Rod 400mm Instrument because the rod has fractured, leaving portions inside patients.
Product
Specialist 2 Intramedullary (SP2 IM) Rod 400mm Instrument (PN 96-6120) The SP2 IM Rod 400mm Instrument (PN 96-6120) is used in both primary and revision P.F.C.¿ SIGMA¿ knee procedures to align the femoral locating device and distal femoral cutting block. It is also used with…
Category
Medical Device
Distribution
40 states
SevereNHTSA·15V654000·2015-10-14
Newmar Recalls 2007-2008 Motorhomes Due to Wheel Bearing Fire Risk
Newmar is recalling 119 model year 2007-2008 motorhomes because tight wheel bearings may overheat and cause a fire.
Product
NEWMAR — NEWMAR DUTCH STAR, MOUNTAIN AIRE, ESSEX
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V652000·2015-10-14
Mercedes-Benz Recalls S63 AMG Sedans and Coupes for Engine Stall Risk
Mercedes-Benz is recalling 2014-2016 S63 AMG vehicles because a software error may cause the engine to stall and fail to restart, increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ AMG S63 4MATIC, AMG S63
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V653000·2015-10-14
The RV Factory Recalls 2015-2016 Avion Azure Motorhomes for Seat Bracket Defect
The RV Factory is recalling 2015-2016 Avion Azure motorhomes because an improperly placed weld on the underfloor seat bracket may cause the bracket to break in a crash, increasing injury risk.
Product
AVION — AVION AZURE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0108-2016·2015-10-14
Beckman Coulter Recalls MICroSTREP plus 1 and 2 Panels for Manufacturing Error
Beckman Coulter is recalling MICroSTREP plus 1 and 2 panels because a manufacturing error may cause antimicrobial degradation and false resistant results.
Product
MICroSTREP plus 1 Panel, Part No. B1027-201 Product Usage: MicroScan MICroSTREP plus panels are designed for use in determining quantitative and/or qualitative antimicrobial agent susceptibility of colonies grown on solid media of aerobic streptococci, including…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0113-2016·2015-10-14
Olympus MAJ-1606 Instrument Channel Adaptors Recalled for Sterility Breach
Olympus is recalling MAJ-1606 Instrument Channel Adaptors due to small puncture marks in sterile packaging that may compromise sterility.
Product
MAJ-1606 Instrument Channel Adaptor; a single use adapter which enables a connection between the endoscope's instrument channel port and the O FP-2 pump's tubing.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0001-2016·2015-10-14
General Mills Recalls Cascadian Farm Frozen Cut Green Beans
General Mills is recalling a limited quantity of frozen Cascadian Farm Cut Green Beans after one package tested positive for Listeria monocytogenes.
Product
Cascadian Farm Organic Cut Green Beans, Net. Wt. 16 oz.
Category
Food
Distribution
Distributed nationwide
HighNHTSA·15V656000·2015-10-14
Toyota Recalls 2016 Tacoma Trucks Due to Knee Air Bag Bolt Issue
Toyota is recalling 2016 Tacoma trucks because incorrect bolts were used to install the driver's knee air bag module, which may loosen over time.
Product
TOYOTA — TOYOTA TACOMA
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·16007·2015-10-14
TCC Cooking Company Recalls CHEFS Vertical Roasters Due to Breakage Hazards
TCC Cooking Company is recalling CHEFS vertical roasters because they can break or shatter, posing burn and laceration hazards. No injuries have been reported.
Product
Vertical roasters
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·15V655000·2015-10-14
Mercedes-Benz Recalls 2014-2015 B-Class Electric Drive Vehicles for Software Defect
Mercedes-Benz is recalling 2,618 model year 2014-2015 B-Class Electric Drive vehicles because a communication error may cause the electric powertrain to shut down, temporarily immobilizing the vehicle.
Product
MERCEDES BENZ — MERCEDES BENZ, MERCEDES-BENZ B-CLASS ELECTRIC, B 250E
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0107-2016·2015-10-14
Siemens SOMATOM Force CT Systems Recalled for Software and Firmware Bugs
Siemens Medical Solutions USA is recalling 21 SOMATOM Force computed tomography systems due to software and firmware bugs.
Product
SOMATOM Force; computed tomography x-ray system. Intended to generate and process cross-sectional images of patients.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15V657000·2015-10-14
Mercedes-Benz Recalls 2015 S-Class Models Due to Seat Belt Installation Error
Mercedes-Benz is recalling 2,580 model year 2015 S550 4Matic, AMG S63, and AMG S65 vehicles because front seat belts may be installed on the wrong side, affecting crash protection.
Product
MERCEDES-BENZ — MERCEDES-BENZ AMG S63, AMG S65, S550 4MATIC
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0022-2016·2015-10-14
Medtronic SureScan Pacemaker ID Cards Mislabel MR Conditional Status
Medtronic is recalling 777 identification cards for SureScan pacemaker patients that incorrectly indicate the entire system is MR Conditional.
Product
Medtronic Medical Device Identification Card for SureScan pacemaker patients. The front of this card identifies the implanted pacing system components currently registered to the patient. The back of the card lists patient's following physician as well as specific…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0020-2016·2015-10-14
Siemens SOMATOM Definition Flash CT Scanner Software Recall
Siemens Medical Solutions USA is recalling 113 SOMATOM Definition Flash CT scanners due to a software bug in version VA48A_SP0 that affects visual warnings and image quality.
Product
SOMATOM Definition Flash; intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral planes taken at different angles.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0021-2016·2015-10-14
Siemens SOMATOM Definition AS CT Scanner Software Recall
Siemens Medical Solutions is recalling 113 SOMATOM Definition AS CT scanners to fix a software bug affecting visual warnings and image quality.
Product
SOMATOM Definition AS, intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral planes taken at different angles.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0023-2016·2015-10-14
GE Healthcare Recalls Centricity PACS IW Due to Missing Images
GE Healthcare is recalling 921 Centricity PACS IW systems worldwide because images may be missing when a specific system parameter is set to a value greater than 1.
Product
Centricity PACS IW by GE Healthcare Dynamic Imaging Solutions is a device that receives medical images (including mammograms) and data from various imaging sources. Images and data can be stored, communicated, processed and displayed within the system or across computer networks…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0109-2016·2015-10-14
Beckman Coulter Recalls MICroSTREP plus Panels Due to Manufacturing Error
Beckman Coulter is recalling MICroSTREP plus 1 and 2 panels because a manufacturing error may cause antimicrobial degradation, leading to false resistant results.
Product
MICroSTREP plus 2 Panel, Part No. B1027-202 Product Usage: MicroScan MICroSTREP plus panels are designed for use in determining quantitative and/or qualitative antimicrobial agent susceptibility of colonies grown on solid media of aerobic streptococci, including…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0110-2016·2015-10-14
Beckman Coulter Recalls Access Free T3 Reagent Kits Due to Filling Errors
Beckman Coulter is recalling Access Free T3 Reagent Kits because they were filled incorrectly and contain insufficient reagents.
Product
Access Free T3 Reagent Kit, P/N A13422 The Access Free T3 assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of free triiodothyronine levels in human serum and plasma using the Access Immunoassay Systems.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0019-2016·2015-10-14
Siemens SOMATOM Definition Edge CT Scanner Software Recall
Siemens Medical Solutions is recalling 113 SOMATOM Definition Edge CT scanners due to a software bug affecting visual warnings and image quality.
Product
SOMATOM Definition Edge; intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral planes taken at different angles.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0008-2016·2015-10-14
Daytrana Methylphenidate Patches Recalled for Defective Delivery System
Noven Pharmaceuticals is recalling Daytrana (methylphenidate) 30 mg patches due to a defective delivery system that failed mechanical peel force specifications.
Product
DAYTRANA — DAYTRANA (METHYLPHENIDATE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·15V643000·2015-10-13
Volvo Recalls 2011-2013 VNL, VAH, and VNM Trucks for Fifth Wheel Defect
Volvo is recalling 2011-2013 VNL, VAH, and VNM trucks because the fifth wheel locking mechanism may fail, potentially causing the trailer to detach.
Product
VOLVO — VOLVO VNM, VNL, VAH
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V642000·2015-10-13
Newmar Recalls 2016 Motorhomes Due to Parking Brake Calibration Defect
Newmar is recalling 86 model year 2016 Bay Star and Canyon Star motorhomes because the parking brake may fail to hold the vehicle or disengage properly.
Product
NEWMAR — NEWMAR BAY STAR, BAY STAR SPORT, CANYON STAR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V644000·2015-10-13
Mack Pinnacle Trucks Recalled for Fifth Wheel Locking Mechanism Defect
Mack is recalling 2011-2014 Pinnacle trucks because the fifth wheel locking mechanism may fail, risking trailer detachment and a crash.
Product
MACK — MACK PINNACLE (CXU), PINNACLE (CHU)
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V648000·2015-10-13
Autocar Recalls 2014-2016 Xpeditor Vehicles Due to Brake Plunger Defect
Autocar is recalling 483 model year 2014-2016 Xpeditor vehicles because a stuck brake plunger may cause dragging brakes and loss of control.
Product
AUTOCAR — AUTOCAR XPEDITOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V649000·2015-10-13
Great Dane Recalls 2016 Trailers Due to Axle Nut Retaining Clip Defect
Great Dane is recalling 2016 Dry Freight and Converter Dolly trailers because axle nut retaining clips may be missing or improperly seated, risking wheel loss and loss of vehicle control.
Product
GREAT DANE — GREAT DANE CONVERTER DOLLY, DRY FREIGHT SEMI-TRAILER
Category
Vehicle
Distribution
Distributed nationwide