State
72,971 recalls have nationwide distribution and so reach South Carolina. 7,117 additional recalls listed South Carolina specifically in their distribution scope.
Of the 7,117 recalls naming South Carolina we have scored against our rubric, 1,268 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,870 (26%) are Severe.
Which agencies issued them
These figures cover only the 7,117 recalls whose distribution notice names South Carolina specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Honda is recalling certain 2025 CR-V Hybrid vehicles because the fuel feed hose may have been improperly installed, allowing fuel to leak. This fails FMVSS 301.
ZRWD infant swings (model S0008A) sold on Amazon are recalled due to suffocation risk from incline angles exceeding safety limits and missing battery hazard warnings. About 3,540 units are affected.
HTP-brand ELU Elite Ultra residential gas boilers are being recalled because the boiler door can fail to seal properly, allowing flames and gases to escape, posing fire and carbon monoxide poisoning hazards that can result in death or serious injury.
Starcraft RV is recalling 45 units of the 2025 Autumn Ridge travel trailer because undersized safety chains could fail, allowing the trailer to separate from the tow vehicle.
Apollo America 51000-600 combination smoke and carbon monoxide detectors can malfunction and fail to alert users to fire or CO leaks, risking smoke inhalation, CO poisoning, or death. Vivint is sending free replacement detectors to all known purchasers.
About 380 Funlio convertible high chairs pose entrapment and fall hazards due to violations of federal safety standards. The opening between seat and tray is large enough for a child to become trapped, and the child restraint system can fail.
NTI Boilers is recalling about 323 NTI-brand TRX Series II residential wall-mounted gas boilers sold in the US because the boiler door can fail to seal properly, posing fire and carbon monoxide poisoning hazards that can result in death or serious injury.
Midea is recalling about 1.7 million U and U+ Window Air Conditioners because pooled water can fail to drain quickly, allowing mold to grow. At least 152 mold reports exist, including 17 reports of consumers experiencing respiratory infections, allergic reactions, coughing, sneezing, and sore throats.
Rinnai America is recalling about 2,030 i-Series Plus gas boilers because the door can fail to seal properly due to incorrect screws, allowing carbon monoxide to escape. No injuries have been reported.
Yamaha is expanding a recall of approximately 352,000 golf car vehicles because the accelerator pedal spring can fail to return to idle, posing a crash hazard. No injuries have been reported to date.
Hobby Toy Hammer Ball sets sold on Amazon contain small balls that violate federal toy safety regulations for children under three and pose a choking hazard. About 2,000 units sold from September 2024 through April 2025 are affected.
DR Power Equipment battery-powered chainsaws are being recalled because the motor controller can overheat during operation, posing fire and burn hazards. About 7,180 units were distributed nationwide.
Direct Scaffold Supply is recalling casters used in multi-purpose baker style scaffolding due to faulty spot welds that can cause caster failure and scaffolding instability, creating a fall hazard. One injury from a caster failure has been reported.
Mercedes-Benz is recalling certain 2022–2025 S-Class, EQE, EQE SUV, EQS, and EQS SUV vehicles because the Acoustic Vehicle Alerting System (AVAS) software may produce an incorrect warning sound while reversing, potentially failing to alert pedestrians.
Specialized Bicycle Components is recalling about 11,100 Globe-branded Haul ST and LT e-bikes due to a telescopic seat post that can break when fully extended, creating a fall hazard. The company has received 13 incident reports including two minor injuries.
Lutron-branded power interfaces for LED tape lights can fail during power surges like lightning strikes, creating a shock hazard. About 1,944 units are affected; no injuries have been reported.
Triple E is recalling 2025 Wonder and Unity motorhomes because incorrectly installed inverter wiring insulation may overheat, increasing the risk of fire.
Glenmark Pharmaceuticals is recalling Carvedilol Tablets USP 25 mg nationwide due to the presence of N-Nitroso Carvedilol I impurity above the recommended acceptable intake limit, resulting from CGMP deviations.
Onkos Surgical is recalling ELEOS Collar Stem components (Model HC-15120-03M) that were packaged and labeled as 13mm modular segmental stems when they are actually 15mm in diameter. This mislabeling could result in implantation of an incorrectly-sized component during limb salvage surgery.
Onkos Surgical is recalling 23 units of ELEOS Collar Stem implants (Model HC-13120-03M) because packages labeled as 13mm contained 15mm diameter implants instead, creating a risk of implant mismatch during surgery.
Glenmark Pharmaceuticals Inc., USA is recalling Carvedilol Tablets USP 12.5 mg due to the presence of N-Nitroso Carvedilol I impurity above the recommended acceptable intake limit, resulting from current Good Manufacturing Practice (CGMP) deviations.
Williams Farms Produce Sales Co., Inc. is recalling Tomato 3 Count products (UPC 0 33383 65504 8) distributed to GA, NC, and SC because the product may contain Salmonella.
Glenmark Pharmaceuticals Inc., USA is recalling Carvedilol Tablets USP 3.125mg due to the presence of N-Nitroso Carvedilol I impurity above the recommended acceptable intake limit. The recall affects 100-count and 500-count bottles distributed nationwide.
Glenmark Pharmaceuticals Inc., USA is recalling Carvedilol Tablets USP 6.25 mg due to the presence of N-Nitroso Carvedilol I impurity above the recommended acceptable intake limit. The recall affects 100-count and 500-count bottles distributed nationwide.
VEPEMVA Nutrition's Endurance Boost with Horny Goat Weed has been recalled because it contains Sildenafil and Propoxyphenylsildenafil, undisclosed active pharmaceutical ingredients. The product was marketed and sold without FDA approval.