South Carolina recalls

Sold nationwide. Maquet is recalling three Percutaneous Insertion Kit products because the packaging may not consistently maintain the sterile barrier. No injuries have been reported. About 271,000 units were distributed in the US and many other countries.

Moderate·FDA·Sep 23, 2026·Maquet3 products

Sold nationwide. GE's Carescape Central Station patient monitoring system may take up to 3 minutes to resume monitoring after a restart. During this gap, clinically important changes in a patient's condition might not be detected right away.

Moderate·FDA·Sep 23, 2026·GE

Sold nationwide. Philips is recalling two patient information system products because a software malfunction can cause the system to freeze and stop responding. The recall includes 7,671 affected units across the two products, which were distributed in the US and internationally. No injuries have been reported.

Moderate·FDA·Sep 23, 2026·Philips2 products

Sold nationwide. Medline's Open Heart Convenience Kit (DYNJ43008N) contains a coronary cannula with a potential sterile barrier breach. If a compromised pouch seal isn't caught before use, the non-sterile device could cause infection or serious complications including blood cell breakdown, blood clots, or organ damage.

Serious·FDA·Sep 23, 2026·Medline

Sold nationwide. Nova Biomedical is recalling five StatStrip glucose meter models, about 44,400 units in total. A software timing issue can cause a meter to keep the previous patient's or control solution's barcode on screen, so a glucose result may be recorded under the wrong patient. The glucose measurements themselves are not affected, and no injuries have been reported.

Serious·FDA·Sep 23, 2026·Nova Biomedical5 products

Sold nationwide. Medline is recalling seven groups of convenience kits because certain lots of sterile applicators may contain fungus (Aspergillus penicillioides). Skin preparation products contaminated with this fungus can cause serious infections, including sepsis, and death. The kits were distributed nationwide, and the FDA has classified this as a Class I recall, its most serious category.

Serious·FDA·Sep 23, 2026·Medline7 products

Sold nationwide. Halyard IV START KIT convenience kits (Lot 1658437) contain applicators contaminated with Aspergillus penicillioides, a fungus. The contamination was found in BD ChloraPrep Clear and FREPP Clear applicators included in the kits. This is a Class I recall affecting 288 units distributed in Nebraska.

Serious·FDA·Sep 23, 2026·AVID MedicalExpanded Sep 30

Sold nationwide. BD Switzerland has recalled multiple models of Alaris Pump Infusion Sets due to discrepancies in performance data attributes. These discrepancies may cause the infusion pump to operate inappropriately. No injuries have been reported.

Serious·FDA·Sep 23, 2026·BD

Sold nationwide. Bard is recalling 2 product lines of short-term straight dialysis catheters, with about 172,500 units affected. The recall is downstream of a related Class I recall, RES 98777, and the filing does not describe the specific hazard. No injuries have been reported.

Serious·FDA·Sep 23, 2026·Bard2 products

Taylor Farms is recalling 25 fresh products because they may be contaminated with Salmonella. The products include pico de gallo, salsas, guacamole, dips, salads, a burrito and a sandwich, sold under the Taylor Farms name and also under Walmart, ADUSA Distribution and BH Bold names. Affected units were sent to several states, including Texas, Illinois, Kentucky, Tennessee, Florida and Rhode Island. No illnesses have been reported.

Serious·FDA·Sep 23, 2026·Taylor Farms25 products

Sold nationwide. Foods Alive organic moringa leaf powder in 8oz pouches may be contaminated with Salmonella. About 1,691 pouches were distributed nationwide and online. No illnesses have been reported so far.

Serious·FDA·Sep 23, 2026·Foods Alive

Sold nationwide. Vitruvias Therapeutics is recalling Thyroid Tablets, USP 1/2 Grain (30 mg) because the tablets are superpotent—meaning they contain higher-than-intended levels of active ingredients. This lot was distributed nationwide. The affected lot number is 504950, expiring 09/30/2026.

Serious·FDA·Sep 23, 2026·Vitruvias Therapeutics

Sold nationwide. Pfizer has recalled one lot of Dopamine HCl injection (40 mg/mL) distributed nationwide due to a lack of assurance of sterility. The affected lot is NL5230, with an expiration date of October 2027. This is a precautionary measure to ensure patient safety.

Moderate·FDA·Sep 23, 2026·Pfizer

Sold nationwide. Inventia Healthcare Limited's chlorthalidone 25 mg tablets (batch RISA24002, expiring 04/2027) failed to meet dissolution specifications, meaning the tablets may not break down properly in the body. This could affect how well the medication works. About 13,567 bottles were distributed nationwide.

Moderate·FDA·Sep 23, 2026·Inventia Healthcare

Sold nationwide. Taro Pharmaceuticals is recalling one lot of Lidocaine Ointment USP 5% because testing found the active ingredient strength was outside acceptable limits. The affected lot was identified during long-term stability testing. No injuries have been reported.

Moderate·FDA·Sep 23, 2026·Sun Pharmaceutical

Sold nationwide. Safecor Health is recalling specific lots of Fluphenazine HCl Elixir 2.5 mg per 5 mL because they failed stability testing, meaning the medication may not maintain its strength or safety over time. The affected lots were distributed nationwide.

Moderate·FDA·Sep 23, 2026·Safecor Health6 products

Sold nationwide. Sun Pharmaceutical is recalling specific lots of Nystatin Cream, USP (15 g tubes) because the medication failed stability testing. This means the cream may not maintain its expected strength or safety over time. The affected lots are AD49605 and AD49606, with expiration dates of 05/31/2027.

Moderate·FDA·Sep 23, 2026·Sun Pharmaceutical

Sold nationwide. Heinz Real - Vraie Mayonnaise 12.5ml single-serving packets contain undeclared ingredients, including mustard. This poses a risk to people with mustard allergies. The affected packets have best-by dates of March 27 or 28, 2027, and were distributed in Canada.

Moderate·FDA·Sep 23, 2026·Heinz

Sold nationwide. Star Meat Delivery Inc. produced approximately 167,639 pounds of raw pork, beef, and goat products without federal inspection and labeled them with a false USDA inspection mark (establishment number EST. 1363). The products were distributed in bulk under the A&D Foods label to retailers and restaurants nationwide. Food produced without inspection may contain harmful bacteria, undeclared allergens, or other contaminants.

Serious·USDA·Sep 22, 2026·A&D Foods

Sold nationwide. Global Mix Inc. is recalling Niwali Tejocote Capsules and Niwali Tejocote Pieces because FDA testing found the products actually contain yellow oleander (Thevetia peruviana), a highly toxic plant. All parts of yellow oleander contain cardiac glycosides that can cause severe or fatal effects including nausea, vomiting, heart rhythm changes, and organ damage.

Serious·FDA·Sep 21, 2026·Global Mix

Sold nationwide. Par Pharmaceutical is recalling two lots of dexmedetomidine HCl injection used in hospitals for patient sedation. The vials contain unwanted particles of cellulose or stopper material that could cause serious blood vessel blockages or clotting if injected into patients. No patient injuries have been reported so far.

Serious·FDA·Sep 18, 2026·Par Health

Sold nationwide. One lot of ICU Medical 0.9% Sodium Chloride Injection (a salt solution) was found to contain 10 mEq Potassium Chloride Injection instead. The vial had the correct outer label but the wrong product inside. This was discovered through a customer complaint.

Serious·FDA·Sep 17, 2026·ICU Medical

Sold nationwide. These translucent green squishy toys contain water beads that expand larger than the legal safety limit. If a child ingests a water bead, it can cause choking, intestinal blockage, vomiting, dehydration, and potentially death.

Serious·CPSC·Sep 17, 2026·Toyworld168

Sold nationwide. Tongyang Cycling's Basecamp model HT-10 bicycle helmets do not meet federal safety standards for impact protection and stability, and may fail to protect your head in a crash. The helmets also contain button cell batteries without required warning labels, creating a poisoning risk if swallowed.

Serious·CPSC·Sep 17, 2026·Tongyang Cycling

Sold nationwide. The infrared heating panels in Sauna360 saunas and kits can short circuit and overheat, creating a risk of fire and serious burns. The company has received 67 reports of overheating, melting, charring, or burning, though no injuries have been reported yet.

Serious·CPSC·Sep 17, 2026·Sauna360

Sold nationwide. The bench seating in Sauna360's Tylö Halmstad and Kiruna Hybrid sauna rooms can collapse, creating a fall hazard. A previous repair offered in October 2025 did not fully resolve the problem. Sauna360 has received 77 reports of bench failures, resulting in six injuries.

Serious·CPSC·Sep 17, 2026·SFactor

Sold nationwide. SHEIN is recalling Pull and Chew Montessori Teething Toys because the silicone strings are longer and smaller than safety standards allow. The strings can reach the back of a child's throat and become lodged, creating a serious choking risk.

Serious·CPSC·Sep 17, 2026·Shein

Sold nationwide. Regfear's BedsPick brand mattresses (12-inch queen size, sold compressed in boxes) fail to meet mandatory federal flammability standards, creating a risk of fire-related injury or death. The mattresses have a white top with either purple or gray sides and were sold on Amazon between February 2025 and May 2026.

Serious·CPSC·Sep 17, 2026·Regfear

Sold nationwide. The black plastic fire hose port on this toy fire truck can come loose and detach, creating a choking hazard for young children. Melissa & Doug has received 26 reports of the port detaching and one report of a minor cut. The toy was sold at Target stores and online from July 2025 through August 2026.

Serious·CPSC·Sep 17, 2026·Melissa & Doug

Sold nationwide. LANCHEZ-branded electric pressure washers lack a ground-fault circuit-interrupter (GFCI) and have a short power cord, which may lead users to rely on extension cords. This creates a serious risk of electric shock or electrocution. About 329 units were sold online between February and June 2026.

Serious·CPSC·Sep 17, 2026·Lanchez