Florida recalls

Bakkavor's Basil Pesto & Mozzarella Pizza may contain small metal fragments in the bread. The metal came from roasted tomatoes supplied by one of the company's ingredient suppliers. The affected pizzas were distributed to nine states: Arizona, California, Connecticut, Florida, Illinois, Michigan, North Carolina, New Jersey, Texas, and Virginia.

American Laboratories is recalling Pepsin 1:3000 Powder (Item #FTI-G0193-00, Lot Code 00160041) because it may be contaminated with Salmonella. The affected powder was distributed to wholesale accounts in multiple states and Australia. No illnesses have been reported so far.

American Laboratories is recalling Pepsin 1:10,000 Powder (Item #FTI-G0193-00, Lot Code 00560021) due to potential Salmonella contamination. The affected product was distributed to wholesale accounts in multiple states and Australia. No illnesses have been reported.

American Laboratories is recalling Pepsin Full Strength Powder (Item #5000545, Lot Code 29460025) due to potential Salmonella contamination. The affected product was distributed to wholesale accounts in multiple states and Australia. No illnesses have been reported.

Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient.

Western Mixers Produce & Nuts, Inc. is recalling Treasured Harvest brand Chilli Spanish Peanuts (25lb bag, lot #260230, expiration 1/23/2027) because glass fragments were found inside a sealed container. One case has been distributed to retail locations across the country.

Western Mixers Produce & Nuts found glass inside sealed containers of First Street Chilli Spanish Peanuts (11oz). The affected products have lot numbers 260422, 260442, or 260543, with expiration dates between February 11–23, 2027. No injuries have been reported.

American Health Packaging is recalling specific batches of Meclizine Hydrochloride 12.5 mg tablets because they failed to meet required tablet specifications. The affected product is Lot #1024852 with an expiration date of 9/30/2026. No injuries have been reported.

Teva Pharmaceuticals is recalling specific lots of Octreotide Acetate 30 mg injectable suspension due to quality control problems found at the manufacturer. The FDA identified deficiencies that mean the sterility of these vials cannot be guaranteed. No injuries have been reported.

Teva Pharmaceuticals is recalling specific lots of Octreotide Acetate injectable suspension (20 mg) due to quality control issues at the manufacturing facility in Greece. The FDA found deficiencies that could affect sterility—the assurance that the medication is free from harmful bacteria and other microorganisms.

Teva Pharmaceuticals is recalling specific lots of Octreotide Acetate injectable suspension due to sterility concerns identified at the manufacturing facility. The FDA found quality system deficiencies that could affect the safety of the medication.

Macleods Pharma USA is recalling Levothyroxine Sodium Tablets USP 150 mcg because they may contain less active ingredient than labeled. This means the medication may not work as intended to treat thyroid conditions. The affected lot is 16240062A with an expiration date of March 2026.

Chiesi USA is recalling specific lots of CUROSURF, a medication given to premature infants to help them breathe. The company cannot confirm that all vials are sterile, which means they may be contaminated. No infections have been reported so far.

Radnostix Gelatin Capsule Packs used with Sodium Iodide I-131 Kit have failed quality specifications. The affected capsules may not perform as intended. Three specific lots distributed nationwide are involved.

Kian Pee Wan capsules, sold online as a dietary supplement for weight gain and appetite, contain two hidden prescription drugs: dexamethasone (a corticosteroid) and cyproheptadine (an antihistamine). These drugs were not listed on the label. Taking these undeclared drugs can cause serious health problems including infections, high blood sugar, psychiatric issues, and withdrawal symptoms if stopped abruptly.

MPINOI brand adult portable bed rails can trap users between the rail and mattress, creating a serious risk of injury or death by asphyxiation. The rails also lack required warning labels. About 200 units were sold on Amazon between December 2025 and February 2026.

The electrical components in DIY Cold Plunge Sauna Heater Kits can overheat and create a fire hazard. The company has received 12 reports of units overheating, though no fires or injuries have occurred yet. The kits were sold online from March 2025 through February 2026.

FUNTOK 24V 2-Seater Ride-On Trucks (model DLS-K03) can overheat and catch fire due to a defective circuit board. The company has received 11 reports of fires, sparking, and smoking. No injuries have been reported yet, but the risk of serious burn injury is significant.

The aluminum shaft on Petzl Nomic and Ergonomic ice climbing axes can break at the handle during use, creating a fall hazard. This affects axes sold between December 2017 and March 2022. Petzl has received 26 reports of shaft breaks but no injuries so far.

CCCEI-branded power strips sold online lack proper safety protection and can overheat and catch fire if too many devices are plugged in. Two units have already sparked and melted. The company is recalling about 5,500 units sold between April 2024 and January 2026.

GLMZZ Fidget Magnet Ball Toy Sets contain high-powered magnets that can be swallowed by children. If multiple magnets are ingested, they can attract each other inside the digestive system, causing perforations, blockages, or twisting of the intestines—which can lead to serious injury or death. The sets were sold on Amazon between February and October 2025.

Sunnyyes LED mini lights contain lithium coin batteries that children can easily access and swallow. The battery compartment screws can come loose, and the packaging lacks required safety warnings. Swallowing these batteries can cause serious internal burns and death.

DuraTrac stainless steel gas connectors sold between May and November 2025 contain a manufacturing defect that can cause gas leaks. These leaks pose a fire hazard. About 196,800 units are affected.

AirClub convertible bassinets (model QX-831) have a defective attachment mechanism that creates a dangerous gap between the bassinet and adult bed mattress. Infants can fall through this opening, causing serious injury or death. About 110,400 units were sold online between October 2023 and December 2025.

Vive Health bed rails can trap users between the rail and mattress, creating a serious risk of asphyxiation. Two deaths have been reported. The recall affects three models: Compact Bed Rail (LVA2009SLV), Bed Rail Collection V (LVA2097SLV), and Bed Rail model LVA1024 purchased on or before August 21, 2023.

4our Kiddies plastic furniture straps (tip restraint kits) can break or degrade over time, allowing furniture to tip over and potentially trap or injure children or elderly people. The plastic brackets and cables fail to meet safety standards, and CPSC has received reports of at least 150 incidents where these straps broke, including three furniture tip-overs.

Nexgrill grill brushes sold at Home Depot can shed small metal wire bristles that may stick to food or the grill surface. If swallowed, these bristles can cause serious internal injuries requiring surgery. The company has identified at least 68 cases where bristles detached, including five people who needed medical care.

Datascope's Battery Charging Station (Model 0998-00-0802) for Cardiosave IABP batteries has a protruding screw in the left bay that can prevent certain batteries from inserting fully and charging properly. The right bay works normally. This affects 28 units distributed in select U.S. states and international locations.

Hologic's Aptima HPV Assay test kits (Master Lot 929785) may produce invalid results or false negatives, meaning they could fail to detect HPV infection. The affected kits were distributed to healthcare facilities in California, Florida, Iowa, Illinois, Missouri, North Carolina, New Mexico, Puerto Rico, and Tennessee.

Diagnostica Stago's STA Liatest D-Di blood test kits are giving inaccurate measurements for D-dimer (a marker used to help rule out blood clots). The kits are showing higher-than-actual results across all test ranges. These kits are used in hospital and reference laboratories on specific analyzer machines.