State

South Carolina product recalls

73,088 recalls have nationwide distribution and so reach South Carolina. 7,145 additional recalls listed South Carolina specifically in their distribution scope.

What the numbers show

Total: 7,145
Critical: 1,278
Severe: 1,882
Most recent: 2026-09-23

Of the 7,145 recalls naming South Carolina we have scored against our rubric, 1,278 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,882 (26%) are Severe.

Which agencies issued them

These figures cover only the 7,145 recalls whose distribution notice names South Carolina specifically. The 73,088 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9276–9300 of 80233

SevereFDA (Devices)·Z-0292-2025·2024-11-20
Trilogy Evo Universal Ventilator Recalled Due to Sensor Malfunction Risk
Trilogy Evo Universal Ventilators (Model DS2000X11B) are recalled because in-line nebulizer configuration in certain locations could cause aerosol accumulation on the internal flow sensor, potentially resulting in inaccurate measurements.
Product
Trilogy Evo Universal Ventilator. Model Number DS2000X11B. Intended for invasive and non-invasive ventilation of pediatric through adult patients weighing at least 2.5 kg in institutional, home, and non-emergency transport settings.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·24E098000·2024-11-20
Lippert Recalls Fifth Wheel Pin Boxes Due to Fastener Issues
Lippert is recalling specific Curt Helux Pin Boxes installed in Lippert 5W Chassis because fasteners may be improperly tightened, increasing crash risk.
Product
TRAILER HITCHES:FIFTH WHEEL ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24E099000·2024-11-20
Agility Fuel Solutions Recalls CNG Fuel Systems Due to Valve Cracks
Agility Fuel Solutions is recalling certain CNG fuel systems because manual cylinder valves may develop stress corrosion cracks, causing a natural gas leak that increases fire risk.
Product
FUEL SYSTEM, OTHER recall
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0305-2025·2024-11-20
Anesthesia workstation piston ventilator may fail before or during use
Draeger Medical is recalling Atlan A350XL anesthesia workstations due to potential piston ventilator failure that may occur before use or during mechanical ventilation.
Product
Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software Version: Not Applicable Component: Not applicable
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0290-2025·2024-11-20
Trilogy Evo O2 Ventilators Recalled for Potential Flow Sensor Malfunction
Philips Respironics recalled 24,249 Trilogy Evo O2 ventilators because in-line nebulizer configurations may allow aerosol deposits to accumulate on the device's flow sensor, potentially causing inaccurate flow measurements.
Product
Trilogy Evo O2. Model Numbers: FP2100X10, DS2100X11B, IN2100X15B, DE2100X13B, IA2100X15B, EU2100X15B, LA2100X15B, EE2100X15B, FX2100X15B, ES2100X15B, ND2100X15B, FR2100X14B, IT2100X21B, JP2100X16B, IN2100X19, EU2100X19. Intended for invasive and non-invasive ventilation of pedi
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0389-2025·2024-11-20
Surgical Instruments Recalled for Loose Metal Flakes in Set-Up Packs
AVID Medical is recalling Halyard GENERAL SET UP PACK medical convenience kits nationwide due to sponge forceps and towel clamps that may shed small metal flakes into patients' surgical sites, risking local reactions and foreign body reactions.
Product
Halyard GENERAL SET UP PACK - Medical convenience kits Model Number: ESJH005-02
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0427-2025·2024-11-20
Surgical forceps and clamps recall due to potential loose metal flakes
AVID Medical is recalling Halyard OR Endovascular Tray surgical kits due to loose metal flakes that could detach from forceps and clamps and potentially enter the surgical site.
Product
Halyard OR ENDOVASCULAR TRAY - Medical convenience kits Model Number: SAMM048-15
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0448-2025·2024-11-20
Medical Convenience Kits Recalled for Potential Loose Metal Flakes in Surgical Instruments
AVID Medical is recalling Halyard MANIFOLD CATH PACK medical convenience kits because sponge forceps and towel clamps may shed metal flakes that could contaminate surgical sites.
Product
Halyard MANIFOLD CATH PACK - Medical convenience kits Model Number: VMED005-03
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0361-2025·2024-11-20
Urine Collection Kit Specimen Containers Recalled Due to Sterility Defect
Medline Industries is recalling over 626,000 urine collection kits due to specimen containers labeled as sterile but identified as non-sterile. The defect may result in unnecessary treatment or prolonged hospitalization.
Product
URINE KIT W/BD CUP, SKU DYLAB1001A; Component No. 503581
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0420-2025·2024-11-20
Surgical instrument kits recalled due to loose metal flakes
AVID Medical is recalling Halyard Upper Extremity Pack surgical kits because sponge forceps and towel clamps may shed small metal flakes. These flakes could enter a patient's surgical site, potentially causing local or foreign body reactions.
Product
Halyard UPPER EXTREMITY PACK - Medical convenience kits Model Number: PANJ002-02
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0346-2025·2024-11-20
Cook Approach CTO Micro Wire Guide recalled for incorrect expiration date labels
Cook Incorporated is recalling Approach CTO Micro Wire Guide devices due to incorrect expiration dates on affected lot labels. The recall affects 2,005 units in the US and 1,145 units overseas.
Product
Approach CTO Micro Wire Guide, Guide Wire, Catalog Prefix CMW; Reference Part Numbers: CMW-14-190-12G CMW-14-190-18G CMW-14-190-25G CMW-14-190-6G CMW-14-300-12G CMW-14-300-18G CMW-14-300-25G CMW-14-300-6G
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0461-2025·2024-11-20
MEERA CL operating table may stop unexpectedly during surgical procedures
The MEERA CL operating table may experience error code 50037 on its IR-Hand Control, causing the table to stop mid-procedure. No injuries have been reported.
Product
MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examination and treatment Item Number: 710001B2
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0416-2025·2024-11-20
Halyard Extremity Pack Surgical Instruments Recalled for Loose Metal Flakes
AVID Medical recalls Halyard Extremity Pack surgical instruments (model MMOK009-03) because small metal flakes may detach from sponge forceps and towel clamps and enter patients' surgical sites. No injuries have been reported.
Product
Halyard EXTREMITY PACK - Medical convenience kits Model Number: MMOK009-03
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0401-2025·2024-11-20
Halyard TOTAL KNEE Medical Convenience Kits Recalled for Loose Metal Flakes
AVID Medical is recalling Halyard TOTAL KNEE kits because sponge forceps and towel clamps may have loose metal flakes that could detach and enter a patient's surgical site, causing local or foreign body reactions.
Product
Halyard TOTAL KNEE - Medical convenience kits Model Number: GRND008-09
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0342-2025·2024-11-20
IV Fluid Bags Recalled Due to Leaking During Filling
The FDA is recalling Imed EVA BAG IV bags after a limited number were found to leak during filling. The affected bags were distributed nationwide and in Canada.
Product
Imed Products Imed EVA BAG, 150 mL, 2-PORTS, REF IM38040; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0331-2025·2024-11-20
VYGON 250 mL IV Fluid Containers Recalled for Leaks During Filling
The Metrix Company is recalling VYGON 250 mL IV fluid containers that have been found to leak during filling. Leaking containers cannot properly contain intravenous fluid.
Product
VYGON 250 mL EMPTY EVA CONTAINER With 2 Ports, REF CMS-9602; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0458-2025·2024-11-20
MEERA CL operating table stops responding during surgery when IR-Hand Control errors occur
The MEERA CL surgical operating table may fail to respond when error code 50037 occurs on its IR-Hand Control, causing the table to stop moving during procedures and resulting in procedural delays.
Product
MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examination and treatment Item Number: 720001F0
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0338-2025·2024-11-20
IV Fluid Bags Recalled Due to Leakage During Filling
The Metrix Company is recalling SECURE 50 mL empty IV containers due to leakage found during filling. A limited number of affected bags have been distributed nationwide.
Product
SECURE 50 mL EMPTY EVA CONTAINER With 2 Ports (Bulk Packed) , REF 66043; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0434-2025·2024-11-20
Surgical instrument kits recalled for loose metal flakes
AVID Medical is recalling Halyard CPT EP PACK surgical convenience kits due to loose metal flakes on forceps and towel clamps. Detached metal flakes could enter surgical sites and potentially cause local tissue reactions or foreign body complications.
Product
Halyard CPT EP PACK - Medical convenience kits Model Number: SHAN442-04
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0349-2025·2024-11-20
Surgical hip procedure kit recalled for incomplete product seals
Medline is recalling CARROLLTON HIP FX surgical kits due to incomplete seals on items within the kit. Affected units contain Lot Number 24EBP466 and were distributed in Tennessee.
Product
CARROLLTON HIP FX Convenience kit used for surgical procedures, SKU SYNJ910003A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0433-2025·2024-11-20
Surgical forceps and clamps recalled due to detachable metal flakes
AVID Medical is recalling Halyard CPT surgical convenience kits because sponge forceps and towel clamps may shed small metal flakes that could contaminate surgical sites. No illnesses have been reported.
Product
Halyard CPT PEDS ADULT CH PACK - Medical convenience kits Model Number: SHAN431-07
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0335-2025·2024-11-20
IV Fluid Container Bags Recalled for Leaking Defect
The Metrix Company is recalling SECURE 100 mL empty EVA containers for IV use due to leaking discovered during filling. Approximately 2,229 cases were distributed to healthcare facilities in the US and Canada.
Product
SECURE 100 mL EMPTY EVA CONTAINER With 2 Ports, REF 66040; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0394-2025·2024-11-20
Medical surgical kits recalled due to loose metal flakes
AVID Medical is recalling Halyard TOTAL KNEE surgical kits (Model EUOR002-05) because sponge forceps and towel clamps may shed small metal flakes that could contaminate surgical sites and cause reactions.
Product
Halyard KIT, TOTAL KNEE - Medical convenience kits Model Number: EUOR002-05
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0405-2025·2024-11-20
Halyard GYN TRAY surgical kits recalled for loose metal flakes
AVID Medical is recalling 136 units of Halyard GYN TRAY surgical kits due to small loose metal flakes that could detach from sponge forceps and towel clamps. These metal fragments could enter a patient's surgical site undetected, causing local or foreign body reactions.
Product
Halyard GYN TRAY - Medical convenience kits Model Number: LANC014-19
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0397-2025·2024-11-20
Halyard surgical kit recalled for loose metal flakes in forceps and clamps
AVID Medical is recalling Halyard KIT, SPINE surgical convenience kits due to loose metal flakes on sponge forceps and towel clamps. The flakes could detach and enter a patient's surgical site, potentially causing local or foreign body reactions.
Product
Halyard KIT, SPINE - Medical convenience kits Model Number: EUOR004-03
Category
Medical Device
Distribution
Distributed nationwide