411 new US recalls this week across food, vehicles, health products, and consumer goods. All data sourced from the U.S. government open recall data, updated daily.
This Week's Highlights
Lone Star Dairy Products LLC recalls Spray Dried Dairy Powder 25 kg bags or 1 metric ton totes
Salmonella spp. identified in finished product testing
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Siluetaya, LLC recalls SiluetaYa Mexican Tejocote Roots Supplement Pieces; 7g/bottl
Product contains yellow oleander
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Mohamed Hagar recalls Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 2
Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).
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StuffbyNainax recalls MR. 7 SUPER 700000 capsules, 1 capsule blister card, Distrib
Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared sildenafil and tadalafil
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Window Glass May Detach from Frame/FMVSS 217
Nova Bus (US) Inc. (Nova Bus) is recalling certain Ricon hidden frame windows sold through Prevost Parts and Prevost Service Center. Please refer to Nova Bus' attached document for specific part number information. Inadequate adhesion around the window frame may cause the glass to detach. As such, t
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Food 107 New Recalls
- Class II The Maros Group, LLC recalls Prickly Pear Jelly. 9 oz (268 g) glass bottle with gold cap. — Undeclared milk.
- Class I Lone Star Dairy Products LLC recalls Spray Dried Dairy Powder 25 kg bags or 1 metric ton totes — Salmonella spp. identified in finished product testing
- Class II JFE FRANCHISING INC recalls " Dumpling Vegetable 4.5 oz — Foreign Object (Glass)
- Class III Pocas International Corp. recalls POPPING BOBA RTD MIXED BERRY HIBISCUS TEA 12 X 13.8OZ — Packaging integrity issue that may compromise product quality .
- Class II JFE FRANCHISING INC recalls " Dumpling Party Tray (20pcs) Vegetable 13 oz — Foreign Object (Glass)
- + 102 more food recalls →
Vehicles 19 New Recalls
- Window Glass May Detach from Frame/FMVSS 217 — Nova Bus (US) Inc. (Nova Bus) is recalling certain Ricon hidden frame windows sold through Prevost Parts and Prevost Service Center. Please refer to Nova Bus' attached document for specific part number information. Inadequate adhesion around the window frame may cause the glass to detach. As such, t
- High Voltage Disconnect Switch May Fail — International Motors, LLC (International) is recalling certain 2022-2027 IC Bus EVSB school buses. The high voltage disconnect switch may fail to shut off power to the battery.
- Fuel Pump May Fail — Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2015-2022 Lexus RC, 2016-2020 GS, and 2022 IS vehicles. The low-pressure fuel pump inside the fuel tank may fail.
- Front Brake Failure — Bombardier Recreational Products, Inc. (BRP) is recalling certain 2025 Can-Am Origin electric motorcycles. A fatigue failure of the front brake caliper support may occur and result in inoperative front brakes.
- Child Seat May Detach from Base/FMVSS 213 — Graco Children's Products Inc. (Graco) is recalling certain SnugRide Turn & Slide and Modes Nest Travel Systems with Snugride Turn & Slide infant child seats. Please refer to Graco's recall report for specific model information. The infant seat carrier may detach from the base in a crash. As such, t
- + 14 more vehicles recalls →
Drugs & Medications 31 New Recalls
- Class II Appco Pharma LLC recalls Prazosin Hydrochloride Capsules, USP, 1mg, 100-count bottle, — cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.
- Class II Amneal Pharmaceuticals, LLC recalls traMADol Hydrochloride Tablets, USP, 50 mg, 500-count bottle — Failed Impurities/Degradation Specifications: N-nitroso-desmethyl-tramadol impurity (NDSRI) was found out of the specification at 24-month stability interval during Long term stability (25¿C/60%RH).
- Class II Appco Pharma LLC recalls Prazosin Hydrochloride Capsules, USP, 2mg, 100-count bottle, — cGMP deviation: detection of Nitrosamine Drug Substance-Related Impurities, N-nitroso-prazosin impurity C (NNP) above acceptable limits.
- Class II K.C. Pharmaceuticals, Inc recalls Artificial Tears Sterile Lubricant Eye Drops (polyvinyl alco — Lack of Assurance of Sterility
- Class II K.C. Pharmaceuticals, Inc recalls Ultra Lubricating Eye Drops (polyethylene 400 0.4%, propylen — Lack of Assurance of Sterility
- + 26 more drugs & medications recalls →
Medical Devices 254 New Recalls
- Class II Medline Industries, LP recalls THORACIC ROBOTS, DYNJ908777B — Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.
- Class II GE Healthcare LLC recalls SIGNA Premier systems — Whole-Body MR scanners used to produce images of the inside of the human body to aid diagnosis of disease may have been manufactured/serviced with ferrous (steel) fittings instead of non-ferrous (brass) fittings on the magnet rear and if system is accessed to perform service while the magnet is ramped, the magnetic field could attract the ferrous fittings potentially resulting in personnel injury.
- Class II Intuitive Surgical, Inc. recalls Brand Name: da Vinci S, Si Permanent Cautery Hook Instrument — Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments
- Class II Medtronic MiniMed, Inc. recalls MiniMed 720G Insulin Pump (MMT-1809, MMT-1810, MMT-1859, MMT — All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.
- Class II Civco Medical Instruments Co. Inc. recalls eTRAX Needle System Starter Kit 18G (for Aurora Trackers), P — There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
- + 249 more medical devices recalls →
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Source: FDA Recalls & Safety Alerts Open Data — public domain U.S. government data. Data covers April 13–April 17, 2026.