State

South Carolina product recalls

73,737 recalls have nationwide distribution and so reach South Carolina. 7,152 additional recalls listed South Carolina specifically in their distribution scope.

What the numbers show

Total: 7,152
Critical: 1,275
Severe: 2,169
Most recent: 2026-10-28

Of the 7,152 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 2,169 (30%) are Severe.

Which agencies issued them

These figures cover only the 7,152 recalls whose distribution notice names South Carolina specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32976–33000 of 80889

HighFDA (Devices)·Z-1226-2020·2020-02-19
Ortho VITROS Chemistry Calibrator Kit 2 Recalled for Potential Sodium Bias
Ortho Clinical Diagnostics is recalling VITROS Chemistry Products Calibrator Kit 2 units due to a potential for negatively biased sodium (Na+) urine results.
Product
VITROS Chemistry Products Calibrator Kit 2- IVD calibrator for VITROS 250/350/5,1 FS/4600/XT 3400 Chemistry Systems and VITROS 5600/XT 7600 Integrated Systems for the quantitative measurement of CHOL, Cl-, ECO2, K+, Na+, and TRIG Product Code: 1662659
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V093000·2020-02-19
Audi Recalls 2019 Q7 Models Due to Side Air Bag Defect
Volkswagen is recalling 2019 Audi Q7 vehicles because side curtain air bags may not inflate properly in a crash, increasing injury risk.
Product
AUDI — AUDI Q7
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1120-2020·2020-02-19
Flowonix Prometra Programmable 20mL Pump Recalled for Firmware Alarm Anomaly
Flowonix Medical Inc is recalling Prometra Programmable 20mL Pumps because a firmware anomaly may prevent the device from sending error notifications or audible alarms during valve system issues.
Product
Prometra Programmable 20mL Pump. Catalog No. 11827 The device is an implantable infusion pump. GTIN-14 00810335020082
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1122-2020·2020-02-19
Flowonix Prometra II Pump Recall for Firmware Alarm Defect
Flowonix Medical Inc is recalling Prometra II 40mL implantable infusion pumps because a firmware anomaly may prevent the device from sending error codes or audible alarms during valve system issues.
Product
Prometra II 40mL Pump. Catalog No. 16827 The device is an implantable infusion pump. GTIN-14 00810335020242
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1151-2020·2020-02-19
MEDTECH ROSA One 3.1 Brain Application Recalled for Image Reconstruction Errors
MEDTECH SAS is recalling 39 units of the ROSA One 3.1 Brain Application because cross-sectional images may not display properly, potentially compromising surgery planning.
Product
ROSA One 3.1 Brain Application
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0834-2020·2020-02-19
Zydus Recalls Ethacrynate Sodium Injection Vials Due to cGMP Deviations
Zydus Pharmaceuticals is recalling 2,207 vials of Ethacrynate Sodium for Injection due to current Good Manufacturing Practice (cGMP) deviations.
Product
Ethacrynate Sodium for Injection, USP, 50mg/vial, Single Dose Vial, Rx Only, Manufactured by: Cadila Healthcare Limited, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 68382-246-01.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1182-2020·2020-02-19
Arrow International Recalls FlexTip Plus Epidural Catheterization Kits
Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.
Product
FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05503-BID
Category
Medical Device
Distribution
37 states
HighFDA (Devices)·Z-1187-2020·2020-02-19
Arrow International Recalls Epidural Catheterization Kits Due to Syringe Failures
Arrow International is recalling 343,105 epidural catheterization kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
Product
EPIDURAL CATHETERIZATION KIT, Product Code AT-05501-LIN
Category
Medical Device
Distribution
37 states
HighNHTSA·20V094000·2020-02-19
BMW Recalls 2014-2019 M6 Gran Coupe for Loose Third Brake Light
BMW is recalling 2014-2019 M6 Gran Coupe vehicles because the third brake light may detach, creating a road hazard and reducing visibility for following traffic.
Product
BMW — BMW M6
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1145-2020·2020-02-19
Philips VesselNavigator Software Recall for DSA Display Defect
Philips is recalling VesselNavigator software due to a defect that displays digital subtraction angiography images without subtraction.
Product
VesselNavigator application used with Philips Azurion (Azurion 7 Series) Software R1.2 and R2.0, and Philips Allura Xper R9, upgraded to Azurion 1.2 M20. System codes: Azurion 7 B12 (722067), Azurion 3 B20 (722068), Azurion 7 M12 (722078), Azurion 7 M20 (722079), Field…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1152-2020·2020-02-19
Respironics V60 Ventilator Recalled for Frozen Touchscreen Failure
Respironics is recalling 2,851 V60 Ventilators because the touchscreen may freeze, preventing clinicians from adjusting therapy settings. This could delay necessary changes, potentially leading to hypercarbia or hypoxemia.
Product
Respironics V60 Ventilator, Service # 850008, REF: 1053613, 1053614, 1053617, 1053614
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1189-2020·2020-02-19
Arrow International Recalls Epidural Catheterization Kits Due to Syringe Failure Risk
Arrow International is recalling 343,105 epidural catheterization kits because the included syringes may fail, potentially causing dural puncture.
Product
EPIDURAL CATHETERIZATION KIT, Product Code BE-05400-DCHH
Category
Medical Device
Distribution
37 states
HighFDA (Devices)·Z-1109-2020·2020-02-19
Terumo Advanced Perfusion System 1 Roller Pump Recall for Shaft Failure
Terumo is recalling 106 Advanced Perfusion System 1 Roller Pumps because the pump shafts may fail, potentially causing the pump to stop during surgery.
Product
Terumo Advanced Perfusion System 1 Roller Pump, 6 Inch, Catalog Number 816571 - Product Usage: is indicated for use for up to 6 hours in the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when used by a…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V095000·2020-02-19
BMW Recalls 2020 X6 Models Due to Rear Spoiler Detachment Risk
BMW is recalling 2020 X6 vehicles because the rear spoiler may detach while driving, creating a road hazard and increasing the risk of a crash.
Product
BMW — BMW X6
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1202-2020·2020-02-19
Arrow International Recalls FlexTip Plus Epidural Catheterization Sets
Arrow International is recalling FlexTip Plus Epidural Catheterization Sets because the included syringes may fail, potentially causing dural puncture.
Product
FlexTip Plus Epidural Catheterization Set, Product Code JC-05400-DCS
Category
Medical Device
Distribution
37 states
HighFDA (Devices)·Z-1204-2020·2020-02-19
Arrow International Recalls Epidural Catheterization Kits Due to Syringe Failures
Arrow International is recalling 343,105 Epidural Catheterization Kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
Product
EPIDURAL CATHETERIZATION KIT, Product Code JC-05400-LB
Category
Medical Device
Distribution
37 states
HighFDA (Devices)·Z-1124-2020·2020-02-19
Flowonix Prometra Implantable Pump Recall for Firmware Alarm Anomaly
Flowonix Medical Inc is recalling Prometra Programmable 20mL implantable infusion pumps due to a firmware defect that may prevent the device from sending error codes or audible alarms during valve system issues.
Product
Prometra Programmable 20mL Pump. Catalog No. 91827 The device is an implantable infusion pump. GTIN-14 00810335020XXX (XXX = in-country language specific)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1150-2020·2020-02-19
Medtech ROSA Brain 3.0 Software Recalled for Image Reconstruction Errors
Medtech SAS is recalling ROSA Brain 3.0 software because cross-sectional images may not display properly, potentially compromising surgery planning.
Product
ROSA Brain 3.0 Application-Brain
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1154-2020·2020-02-19
Respironics Ventilator Touchscreen Recall Due to Unresponsive Controls
Respironics is recalling V60/V680 ventilator touchscreens that may freeze and fail to respond to touch commands, potentially delaying necessary therapy adjustments.
Product
Respironics RP-Touch Screen, V60/V680 Ventilator Serviced with Touchscreen RP Kit 453561511951 containing a touchscreen labeled as raw part number 1132318 Revision C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1107-2020·2020-02-19
bioMerieux Recalls VIDAS Varicella Zoster IgG Antibody Test Kits
bioMerieux is recalling VIDAS Varicella Zoster IgG antibody kits due to potential invalid calibrations or false positive results.
Product
VIDAS Varicella Zoster IgG (VZG) antibody IVD, kit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1155-2020·2020-02-19
Respironics V680 Ventilator Recalled for Unresponsive Touchscreen
Respironics is recalling 190 V680 Ventilators because the touchscreen may freeze, preventing clinicians from adjusting therapy settings and potentially causing delayed treatment.
Product
Respironics V680 Ventilator, Service # 850011, (OUS Only)
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·20074·2020-02-19
Contigo Recalls 5.7 Million Kids Water Bottles Due to Choking Hazard
Contigo is reannouncing a recall of 5.7 million kids water bottles because the clear silicone spout can detach, posing a choking hazard to children.
Product
Contigo Kids Cleanable Water Bottles
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1217-2020·2020-02-19
Arrow International Recalls FlexTip Plus Epidural Catheterization Kits
Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.
Product
FlexTip Plus Epidural Catheterization Kit, Product Code YC-02220
Category
Medical Device
Distribution
37 states
HighFDA (Devices)·Z-1207-2020·2020-02-19
Arrow International Recalls FlexTip Plus Epidural Catheterization Kits
Arrow International is recalling FlexTip Plus Epidural Catheterization Kits due to potential syringe failures that could cause dural puncture.
Product
FlexTip Plus Epidural Catheterization Kit, Product Code MP-17019-TKP
Category
Medical Device
Distribution
37 states
HighFDA (Devices)·Z-1121-2020·2020-02-19
Flowonix Prometra II Pump Recall for Firmware Alarm Anomaly
Flowonix Medical Inc is recalling Prometra II 20mL implantable infusion pumps due to a firmware defect that may prevent the device from sending error codes or audible alarms for valve system issues.
Product
Prometra II 20mL Pump. Catalog No. 13827 The device is an implantable infusion pump. GTIN-14 00810335020228
Category
Medical Device
Distribution
Distributed nationwide