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Safety · Official FDA Data
The latest food, drug, and medical-device recalls reported to the U.S. FDA — with severity class, the reason, and affected products. Live data, updated through the day.
D'Dioses Fruit Pops, Inc.
Product: Ice Pop, D'Dioses Nuez, 1 Bar (81.7 g), with UPC 827912008548
Reason: May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
FDA recall #H-1166-2026 · Ongoing
D'Dioses Fruit Pops, Inc.
Product: Ice Pop, D'Dioses Tamarindo, 1 Bar (81.7 g), with UPC 827912008593
Reason: May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
FDA recall #H-1172-2026 · Ongoing
Nutricia North America
Product: functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY NET WT. 12 OZ (341g) case UPC 8 57858 00453 3, package UPC 8 57858 00450 2
Reason: Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.
Chiesi USA, Inc.
Product: CLEVIPREX (clevidipine injectable emulsion) 50 mg/100 mL (0.5 mg/mL), 10 Single Use Vials, Rx Only, Manufactured for: Chiesi USA, Inc., Cary, NC 27518, by Fresenius Kabi, Graz, Austria, NDC 10122-611-10.
Reason: Lack of Assurance of Sterility
FDA recall #D-0689-2026 · Ongoing
Bell Pharmaceuticals, Inc
Product: QC Quality Choice, Carbamide Peroxide, 6.5%, 0.5 FL. OZ. (15 mL) a) Washer Bulb included (NDC 63868-026-15); b) 1 bottle (NDC 63868-027-16), Distributed by C.D.M.A., Inc., 43157 W. Nine Mile, Novi, MI 48376.
Reason: SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
FDA recall #D-0680-2026 · Ongoing
Orthofix U.S. LLC
Product: Orthofix MINIRAIL, STANDARD LENGTHENER Model/Catalog Number: M101, Unilateral orthopedic/trauma external fixation device
Reason: Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111
FDA recall #Z-2729-2026 · Ongoing
Boston Scientific Corporation
Product: Rapid Refill Continuous Injection System, UPN M00566001
Reason: Devices contain recalled Medline Namic Angiographic Control Syringe with Rotating Adaptor. There is a risk of syringe loosening or disconnecting from the manifold, resulting in loose connection or complete disconnection. May lead to difficulty connecting syringe, inability to aspirate or inject properly, fluid leakage, or separation of the syringe from the system, potentially requiring device exchange and prolonging the procedure.
FDA recall #Z-2725-2026 · Ongoing
Data source: U.S. Food & Drug Administration (FDA) — openFDA enforcement API. Also see our vehicle recall check and consumer product recalls. Our methodology.
FDA recall #H-1152-2026 · Ongoing
D'Dioses Fruit Pops, Inc.
Product: Ice Pop, D'Dioses Arroz con Leche, 4 oz (85 g), with UPC 710594511843
Reason: May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
FDA recall #H-1160-2026 · Ongoing
Fayus Inc.
Product: OLA-OLA POUNDED GROUNDNUTS (INTWILO) NET WT. 32 oz., 2 lbs. (0.907 kg) Distributed by: Yusol International Foods Sacramento, CA 95828 Product of USA INGREDIENTS: Pounded Groundnuts (Intwilo) UPC: 650655764330
Reason: Undeclared peanuts
FDA recall #H-1175-2026 · Ongoing
GELLERT GLOBAL GROUP
Product: Ruby, Artichoke Hearts Quartered, 5 LB 8 OZ (2500 G) DRAINED WT 3 LBS 6 OZ (1550G), Can, 6 cans per case, Store in dry conditions .
Reason: Foreign material (Glass) was found in the product.
FDA recall #H-1176-2026 · Ongoing
D'Dioses Fruit Pops, Inc.
Product: Ice Pop, D'Dioses Fresa Leche, 4 oz (85 g), with UPC 710594511850
Reason: May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
FDA recall #H-1159-2026 · Ongoing
D'Dioses Fruit Pops, Inc.
Product: Ice Pop, D'Dioses Mango, 3.7 oz (81.7 g), with UPC 827912008494
Reason: May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
FDA recall #H-1171-2026 · Ongoing
D'Dioses Fruit Pops, Inc.
Product: Ice Pop, D'Dioses Limon, 4 oz (85 g), with UPC 710594511836
Reason: May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
FDA recall #H-1169-2026 · Ongoing
D'Dioses Fruit Pops, Inc.
Product: Ice Pop, D'Dioses Cookies Cream, 1 Bar (81.7 g), with UPC 710594511362
Reason: May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
FDA recall #H-1167-2026 · Ongoing
D'Dioses Fruit Pops, Inc.
Product: Ice Pop, D'Dioses Pistachio, 1 Bar (81.7 g), with UPC 827912008487
Reason: May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.
FDA recall #H-1165-2026 · Ongoing
Frutas y Hortalizas del Sur S.A.
Product: Organic Whole Blueberries, Net Wt 10 oz (284g) plastic bag, packed in 8 bags per case of 10 oz each. Keep Frozen
Reason: Potential E. coli O145:H28 Contamination
FDA recall #H-1181-2026 · Ongoing
Bell Pharmaceuticals, Inc
Product: Clinere, Carbamide Peroxide, a) 2 bottles of Clinere Carbamide Peroxide (2 x 0.50 mL) 6.5%, 0.5 fl. oz. (15 mL); b) 1 bottle of Clinere Carbamide Peroxide (0,50 fl. oz. (15 mL), Dist. by: Quest Products LLC, Pleasant Prairie, WI 53158, NDC 68229-102-01.
Reason: SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
FDA recall #D-0679-2026 · Ongoing
Bell Pharmaceuticals, Inc
Product: LEADER, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL), a) Kit -1 RUBBER BULB SYRINGE, 0.5 FL OZ DROPS, (NDC 70000-0689-1); b) 1 bottle (NDC 70000-0688-1), DIST. BY CARDINAL HEALTH, DUBLIN, OH 43017.
Reason: SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
FDA recall #D-0685-2026 · Ongoing
Bell Pharmaceuticals, Inc
Product: FAMILY Wellness, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL), Kit - Washer Bulb Included, (NDC 55319-835-01), DISTRIBUTED BY: MIDWOOD BRANDS LLC, 500 VOLVO PKWY, CHESAPEAKE, VA 23320.
Reason: SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
FDA recall #D-0683-2026 · Ongoing
CareFusion 213, LLC
Product: BD ChloraPrep Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol), 60 x 1 mL applicators/carton, 0.03fl oz (1 mL) each, STERILE SOLUTION, CareFusion 123, LLC, El Paso, TX, subsidiary of Beckton, Dickson and Co. NDC 54365-400-31
Reason: Lack of Assurance of Sterility: Affected product may exhibit an open or incomplete seal on the packaging of the applicator
FDA recall #D-0690-2026 · Ongoing
Bell Pharmaceuticals, Inc
Product: CAREone, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), Bottle, NDC 72476-838-34, DISTRIBUTED BY: FOODHOLD U.S.A, LLC, LANDOVER, MD 20785.
Reason: SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
FDA recall #D-0688-2026 · Ongoing
Padagis US LLC
Product: Nystatin Cream USP, (100,000 USP Nystatin Units), NET WT 15 g, Rx only, 15 g tube, Manufactured by Padagis, Yeruham, Israel, NDC 45802-059-35
Reason: Subpotent Drug: Low out of specification assay results performed during long-term stability testing.
FDA recall #D-0677-2026 · Ongoing
Abiomed, Inc.
Product: ABIOMED Impella CP Set, Pump Set Code 0048-0003, containing BIOMED Impella Introducer, 14 Fr, 13 cm & 25 cm, Product Code 0052-3046. heart pump and accessories
Reason: A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
FDA recall #Z-2682-2026 · Ongoing
Papablic Inc
Product: Papablic Replacement Brush Heads. Model Number: PAPA317AA.
Reason: Potential for brush heads to break.
FDA recall #Z-2734-2026 · Ongoing
Papablic Inc
Product: Papablic Replacement Brush Heads. Model Number: Papablic18B
Reason: Potential for brush heads to break.
FDA recall #Z-2733-2026 · Ongoing
Abiomed, Inc.
Product: ABIOMED Impella CP Introducer Kit 14 Fr, 13 cm, Pump Set Code 0052-0038, containing Kit, 14Fr Introducer, 13cm, Long Taper, Introducer Product Code 0052-3052. heart pump and accessories
Reason: A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
FDA recall #Z-2685-2026 · Ongoing