State
73,388 recalls have nationwide distribution and so reach South Carolina. 7,145 additional recalls listed South Carolina specifically in their distribution scope.
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 2,166 (30%) are Severe.
Which agencies issued them
These figures cover only the 7,145 recalls whose distribution notice names South Carolina specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Renaissance Food Group is recalling Fiesta Corn (10 oz) after positive test results confirmed Listeria monocytogenes in the finished product. All products made with the same components are affected.
Renaissance Food Group is recalling Mild Guacamole Blender products due to positive test results for Listeria monocytogenes. The affected products were distributed in Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling 106 units of Seasoned Squash Onion & Dill due to detection of Listeria monocytogenes. Products were distributed to Alabama, Georgia, and South Carolina.
Philips Respironics Amara View Full-Face Mask lacks critical safety warnings about magnetic components for patients with implantable medical devices. The Class I recall affects 5.6 million units worldwide.
Philips Respironics is recalling the Therapy Mask 3100 NC/SP because the product lacks warnings about magnetic components that may affect patients with implantable devices or metallic splinters in the eyes.
Renaissance Food Group is recalling Large Medium Salsa (13 oz) after positive test results for Listeria monocytogenes were detected in finished product. All products made with the same components are included in the recall.
Philips Respironics is recalling Wisp and Wisp Youth nasal masks because they lack warnings about magnetic components that could interfere with implanted medical devices or cause eye injuries from metallic splinters.
Renaissance Food Group is recalling Hamburger Fixin's (10 oz units) distributed in Alabama, Georgia, and South Carolina due to positive test results for Listeria monocytogenes in the finished product.
Renaissance Food Group is recalling Tri-Pepper Blend (7 oz units) due to positive test results for Listeria monocytogenes. All products manufactured with the same components are included in the recall.
Renaissance Food Group is recalling Spicy Guacamole Blender products because positive test results confirmed Listeria monocytogenes contamination in the finished product.
Renaissance Food Group is recalling Hatch Chile Guacamole Blender due to positive test results for Listeria monocytogenes. Products were distributed to Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Diced Red Onion (10 oz units) distributed to Alabama, Georgia, and South Carolina due to positive test results for Listeria monocytogenes in finished product.
Renaissance Food Group is recalling diced bell pepper and white onion products due to positive test results for L. monocytogenes. The recalled products were distributed in Alabama, Georgia, and South Carolina.
Cipla recalls Arformoterol Tartrate Inhalation Solution due to environmental monitoring failure affecting sterility assurance.
Eden's Answers Inc is recalling Sprigs Lil Ones Sleepy Time herbal supplement due to high bacterial growth in the product. Consumers should stop using it immediately.
IN MY BATHROOM LLC is recalling 485 units of the Seago SG-153 handheld UV-C germicidal wand nationwide due to excessive ultraviolet-C radiation. Consumers should stop using the device and contact the manufacturer for instructions.
Zimmer, Inc. is recalling certain G7 Acetabular System acetabular shells (52 MM and 60 MM) because the outer sterile package has corner walls thinner than specification, which could crack during transit and potentially lead to surgical complications or infection.
Wright Medical Technology recalls 32 units of Stryker EVOLVE Proline Stem due to labeling mismatch: outer packages are labeled with one stem size but contain a different size. Surgeons should verify device size before implantation.
Blue Bird is recalling 2023 Vision and All-American transit buses because the entrance door handrail diameter is too small to meet ADA standards, posing a slip and fall risk.
Wright Medical is recalling EVOLVE Proline Stem devices due to labeling errors where the outer package does not match the device inside. Affected devices are size-mismatched, which could lead to incorrect surgical placement.
Hologic recalls 233 BioZorb LP Markers nationwide due to removable labels showing incorrect expiration dates. Implants labeled with January 2022 dates may be mistakenly used after their actual July 2024 expiration.
WFM 365 Organic Creamy Caesar dressing is recalled because the product does not declare wheat and soy allergens on its label. Consumers with wheat or soy allergies should not consume this product.
Synthes is recalling Hammertoe Continuous Compression Implant (CCI) Kits because the drill pin is incompatible with the included drill template, which may delay surgery or cause soft tissue damage and adverse tissue reactions.
2022 Volkswagen ID.4 vehicles have rearview cameras that may be delayed or deactivated, reducing rear visibility and increasing the risk of crashes. Dealers will provide a free software update.
Philips has recalled MR Patient Care Portal 5000 desktop units (Model 453564792561) due to intermittent audio failure. The device may fail to produce audio, and standard troubleshooting does not reliably resolve the issue.