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ASK Foods Inc is recalling Publix brand Rice & Pigeon Peas (32 oz containers) because they contain soy that is not listed on the label. The product was sold in Florida. People with soy allergies could have a serious reaction if they eat this product.

Moderate·FDA·Jan 21, 2026

House Of Flavors banana pudding ice cream (3-gallon size) contains soy lecithin that is not listed on the label. This poses a risk to people with soy allergies. The affected product was distributed across multiple states.

Moderate·FDA·Jan 21, 20262 products

Cipla USA is recalling certain pre-filled syringes of Lanreotide Injection 120 mg because they may contain particulate matter (small particles) in the solution. The affected syringes have specific lot numbers and expiration dates between October 2026 and March 2027. No injuries have been reported so far.

Moderate·FDA·Jan 21, 2026

Gold Star Distribution is recalling 27 over-the-counter products, including pain relievers, cold and flu medicines, antacids, cough drops, skin and lip care, petroleum jelly, rubbing alcohol and mouthwash. The products were stored or distributed from a facility with insanitary conditions, including rodent exposure and activity. No injuries have been reported.

Moderate·FDA·Jan 21, 202627 products

Encon Safety Products is recalling specific lots of AQ 120 GFEW Aquarion Preserved Cartridges due to manufacturing process deviations that do not meet FDA standards. The cartridges were distributed nationwide. No injuries have been reported.

Moderate·FDA·Jan 21, 2026·Encon Safety Products

One bottle of Alvogen Thyro-Tabs 150mcg levothyroxine tablets (Lot MHA21825) was found to contain 88mcg tablets instead of the labeled 150mcg strength. This mix-up affects only a single bottle distributed nationwide. No injuries have been reported.

Moderate·FDA·Jan 21, 2026·Alvogen

Advanced Pharmaceutical Technology is recalling TESTO-100 CIII testosterone pellets (Lot P-22-3, expiration 06-2027) because they may not be sterile and could be contaminated with harmful microbes. These are prescription implant pellets used for testosterone replacement therapy. The recall affects 22,843 pellets distributed in Georgia, New York, Texas, Puerto Rico, the United Kingdom, Malta, and Greece.

Moderate·FDA·Jan 21, 2026·Advanced Pharmaceutical Technology

Sun Pharmaceutical has recalled three lots of clindamycin phosphate 1% topical solution due to failed quality tests. The affected batches contain higher-than-acceptable impurities and may not contain the correct amount of active ingredient, which could reduce effectiveness.

Moderate·FDA·Jan 21, 2026

Taro Pharmaceuticals is recalling specific lots of fluocinolone acetonide topical solution (0.01%) because testing found higher-than-allowed levels of an impurity. The affected lots were distributed nationwide. No injuries have been reported.

Moderate·FDA·Jan 21, 2026

Adams Manufacturing recalled Adirondack-style resin patio chairs sold at Lowe's and Home Depot because they can crack and collapse during use, creating a fall and injury risk. About 6,100 chairs are affected, sold from August through October 2025 in multiple colors.

Moderate·CPSC·Jan 15, 2026

Energizer is recalling about 4,100 Large Power Indicator Lanterns (model BGAAL9) with June 2024 date codes because the lithium-ion batteries can overheat and cause burns. One overheating incident has been reported, though no injuries so far.

Moderate·CPSC·Jan 15, 2026

The 14-gauge Tuohy needle included in certain Codman CereLink ICP Sensor Basic Kits may have corrosion stains on its surface. These kits are used by hospitals and surgical centers for monitoring intracranial pressure during brain procedures. Integra LifeSciences is recalling specific lot numbers distributed worldwide.

Moderate·FDA·Jan 14, 20262 products

Philips MX40 patient monitors may lose wireless connection to the PIC iX central station when moving between certain access points if the signal strength changes rapidly. This could interrupt patient data transmission to clinical staff.

Moderate·FDA·Jan 14, 2026

Securitas Healthcare found a firmware problem in certain Arial 900 MHz Call Stations that may stop them from sending a low battery alert to the Arial Wireless Emergency Call System before the battery fails. The recall covers 2 products, models CSK200-900 and CSK200-900MR, with firmware version 1.6.3, and no injuries have been reported.

Moderate·FDA·Jan 14, 2026·Securitas Healthcare2 products

Abiomed has recalled 2 units of the Impella 5.5 with SmartAssist S2 heart pump device because the devices were shipped in incorrect outer box cartons. This packaging error may affect proper device identification and handling. No injuries have been reported.

Moderate·FDA·Jan 14, 2026

Sophysa's Pressio 2 ICP Monitoring System (Model PSO-4000) may unexpectedly reboot during use. This device is used in hospitals to measure pressure inside the skull. The reboots could interrupt critical monitoring of patients.

Moderate·FDA·Jan 14, 2026·Sophysa

A software issue in certain BD Pyxis ES Enterprise Server systems may prevent timely updates of patient, medication, and related information from reaching the dispensing cabinets. This could delay access to critical data in healthcare settings. BD and the FDA are working to address the problem.

Moderate·FDA·Jan 14, 2026

Certain Beckman Coulter UniCel DxL 600 analyzers may fail to restart properly after shutdown due to a communication issue. When this happens, the analyzer cannot process patient samples or quality control checks, which can delay test results.

Moderate·FDA·Jan 14, 20262 products

Meridian Bioscience's Revogene C. difficile diagnostic test (a lab assay used with the Revogene instrument) may show declining accuracy over time in certain lots. This could produce false-negative results, meaning the test might not detect C. difficile infection when it is present.

Moderate·FDA·Jan 14, 2026·Meridian Bioscience

Applied Medical Resources has recalled certain Kii Low Profile trocar units because the blade obturator may extend beyond its proper length after assembly. This defect could affect the device's safe function during use. No injuries have been reported.

Moderate·FDA·Jan 14, 2026·Applied Medical Resources

Roche Diagnostics has recalled certain lots of the Elecsys Anti-TSHR blood test due to inconsistent results across different laboratory instruments and variations between calibrator batches. These issues could lead to incorrect or delayed thyroid diagnosis and treatment.

Moderate·FDA·Jan 14, 2026·Roche Diagnostics

Philips Healthcare has recalled certain Incisive CT scanners due to an unstable internal connection in the floating sensor. This instability may cause the scanner to produce incomplete or compromised scans. The issue affects 35 devices distributed across the U.S. and its territories, and no injuries have been reported.

Moderate·FDA·Jan 14, 2026

Siemens LUMINOS Lotus Max and Luminos dRF Max X-ray systems with software version VF11 may show incorrect collimation (beam positioning) when quickly switching between organ programs. This affects only systems with a bucky wall stand for mobile detectors and no ceiling stand.

Moderate·FDA·Jan 14, 2026

Vision RT identified that instructions for the AlignRT InBore radiation therapy system omitted required information about its six Class 1 lasers and their specifications. The missing details are required by federal laser safety regulations. No injuries have been reported.

Moderate·FDA·Jan 14, 2026·Vision RT

Meijer Steam Distilled Water in 1-gallon plastic jugs with red lids may contain floating black foreign material. The affected product was distributed to stores in Illinois, Indiana, Kentucky, Ohio, Michigan, and Wisconsin with a sell-by date of October 4, 2026.

Moderate·FDA·Jan 14, 2026

MAYEJ Italian Parsley packaged in 24lb boxes has been recalled due to potential contamination with Cyclospora cayetanensis, a parasite that can cause foodborne illness. About 1,288 boxes were distributed nationwide. No illnesses have been reported so far.

Moderate·FDA·Jan 14, 2026·MAYEJ

Ziyad is recalling two Baraka products: Baraka French Style Puff Pastry in 1 lb and 1.5 lb sizes, and Baraka Gourmet Pastry Kunafe in a 6.7 oz size. The products may contain partially hydrogenated oils. No injuries have been reported, and the products were distributed nationwide.

Moderate·FDA·Jan 14, 20262 products

McCain is recalling two frozen potato products because they may contain small pieces of clear hard plastic. The recall covers 2 products, sold as Ore-Ida Tater Tots shaped potatoes (30 lb case) and Sysco Imperial Potato Tater Barrel (6 bags of 5 lb each), with about 38,850 cases affected. No injuries have been reported, and the products were distributed in many Western, Southern and Midwestern states.

Moderate·FDA·Jan 14, 2026·Ore-Ida2 products

D. Coluccio & Sons Inc. is recalling Sapori Amaretti Almonds 175 g cookies because they contain elevated levels of hydrocyanic acid, a naturally occurring compound in almonds that can be harmful at high levels. Two specific lots are affected with best-before dates of February 5, 2026 and September 3, 2026.

Moderate·FDA·Jan 14, 2026·Sapori

Rovira is recalling six cracker products because they contain the food colors FD&C Yellow #6 and FD&C Red 40, which are not listed on the label. The products are sold as Snack Crackers 100to en boca (ciento en boca), Tempting Crackers, Vanilla Econo, Vanilla Treats, Tita Crackers, and Great Value Vainilla Crackers, the last of which is sold under the Great Value name. They were distributed in Georgia, Texas, Massachusetts, Illinois, Maryland, the U.S. Virgin Islands, Puerto Rico, Panama, and the British Virgin Islands. No illnesses have been reported.

Moderate·FDA·Jan 14, 20266 products