Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

1276–1300 of 26027

SevereFDA (Food)·H-0591-2026·2026-04-01
Trader Joe's Japanese Style Fried Rice recalled for glass fragments
Ajinomoto Foods North America Inc. is recalling Trader Joe's Japanese Style Fried Rice with Edamame, Tofu, and Hijiki Seaweed (1 lb. bags) due to glass fragments 1–3 cm long and 2–4 mm wide found in the product.
Product
Item 5650173 Trader Joe's Japanese Style Fried Rice with Edamame, Tofu, and Hijiki Seaweed. SKU #097908. Net wt. 1lb. per bag. Retail bag UPC 00979085. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 24/1lb. bags per ca
Category
Food
Distribution
43 states
SevereFDA (Food)·H-0630-2026·2026-04-01
Lucerne 2% Cottage Cheese recalled for metal fragments
Lucerne 2% Cottage Cheese 24 oz. tubs are being recalled due to the potential presence of metal spring fragments. Consumers who have purchased affected product should not consume it.
Product
Lucerne 2% Cottage Cheese 2% Milkfat Small Curd Vitamin A Added Grade A. Net wt.24oz. Perishable and keep refrigerated. Consumer package is a plastic cup with foil lid and clear plastic lid. UPC 0 21130 07662 8. Distributed by Lucerne Foods, Inc PO Box 99, Pleasanton, CA. Produ
Category
Food
Distribution
5 states
SevereFDA (Devices)·Z-1576-2026·2026-04-01
ProGuide Chronic Dialysis Catheters Recalled for Design Defect Risk
Merit Medical Systems is recalling ProGuide Chronic Dialysis Catheters due to a design defect in the sheath introducer that may not split properly. This could lead to hemorrhage, blood clots, or loss of vascular access.
Product
ProGuide Chronic Dialysis Catheters, REF: DC01455550/C, DC21452419/C, DC21452419-NE5/C, DC21452823-NE5/C, DC21454035/C, DC21455550/C
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0618-2026·2026-04-01
Basil Pesto and Mozzarella Pizza recalled for metal fragments
Bakkavor is recalling Basil Pesto & Mozzarella Pizza due to metal fragments discovered in the product. The contamination originated from roasted tomatoes supplied by an ingredient supplier.
Product
Basil Pesto & Mozzarella Pizza NET WT. 13.90OZ (394g) UPC 8 57919 00785 5 Distributed by: Grocery Delivery E-Services New York, NY 10005
Category
Food
Distribution
10 states
SevereFDA (Devices)·Z-1577-2026·2026-04-01
16F Splittable Sheath Introducer Recalled Due to Splitting Defect
Merit Medical's 16F sheath introducers may fail to split properly, posing risks of hemorrhage, foreign body retention, and blood clots during vascular procedures. Approximately 368,264 units distributed worldwide are affected.
Product
16F Dual Valved Splittable Sheath Introducer (bulk, non-sterile), REF: FCL-174-00/B
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1566-2026·2026-04-01
Flexible Cryoprobe Surgical Instruments Recalled for Potential Rupture During Use
Erbe USA Inc is recalling 64,216 Flexible Cryoprobes used in surgery because they may rupture or burst during activation. Affected units were distributed nationwide.
Product
Flexible Cryoprobe (OD 1.1mm, L1.15mm) w/ oversheath (OD2.6mm, L817mm) REF: 20402-401 STERILE EO. For surgical use
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0647-2026·2026-04-01
SiluetaYa Mexican Tejocote Roots Supplement Pieces Recalled for Yellow Oleander
SiluetaYa Mexican Tejocote Roots Supplement Pieces (7g bottles, Lot US1220) are recalled because the product contains yellow oleander, a toxic substance. The product was distributed online to consumers in AZ, CA, NM, NY, TX, and UT.
Product
SiluetaYa Mexican Tejocote Roots Supplement Pieces; 7g/bottle; Dietary Supplement, UPC#: 7500464462411, Lot: US1220 " Expiration Date: 06/2027
Category
Food
Distribution
6 states
SevereFDA (Food)·H-0593-2026·2026-04-01
Ajinomoto Teppanyaki Style Vegetable Fried Rice recalled for glass fragments
Ajinomoto Foods North America is recalling Teppanyaki Style Vegetable Fried Rice due to the presence of glass fragments ranging from 1–3 cm long. Consumers should not eat affected products and should discard or return them.
Product
Item 5650883 Ajinomoto Teppanyaki Style Vegetable Fried Rice - Japanese-style fried rice made with colorful vegetables in an aromatic garlic butter sauce. There are 6/9oz. bags per box or 54oz per box. Retail box UPC 071757508835. Product packaging is flexible bags in a master c
Category
Food
Distribution
43 states
SevereFDA (Devices)·Z-1617-2026·2026-04-01
Philips Respironics Trilogy Evo Ventilator Tidal Volume Discrepancy Recall
Philips Respironics Trilogy Evo Universal ventilators may have tidal volume discrepancies when used with non-pneumatic nebulizers. Approximately 113,717 units distributed worldwide are affected by this Class I recall.
Product
Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00. Continuous home-use ventilator device.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1567-2026·2026-04-01
Flexible Cryoprobes May Rupture During Surgical Activation
Erbe USA Inc recalls 8,284 flexible cryoprobes used in surgical procedures. The devices may rupture or burst during activation, posing a risk to patient safety.
Product
Flexible Cryoprobe (OD 1.7mm, L1.15mm) REF: 20402-410. For surgical use
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0616-2026·2026-04-01
Slow Roasted Diced Tomatoes Recalled for Possible Metal Fragments
Sevillo Fine Foods is recalling Slow Roasted Diced Tomatoes (24 lb bulk packages, UPC 00823338008216) because the product may contain metal fragments.
Product
Slow Roasted Diced Tomatoes (SKU 821, UPC 00823338008216). Frozen. Shelf life: 365 days (frozen) from date of manufacture; 30 days (refrigerated, unopened); 7 days (refrigerated, opened). Plastic poly liner inside cardboard box (bulk). Net weight: 24 lbs. Firm: Sevillo Fine Foods
Category
Food
Distribution
2 states
SevereFDA (Devices)·Z-1615-2026·2026-04-01
Philips Trilogy Evo O2 Ventilator Breathing Support Discrepancy with Non-Pneumatic Nebulizers
Philips Respironics Trilogy Evo O2 ventilators may not deliver the correct breathing support when used with non-pneumatic nebulizers. Verify nebulizer compatibility and contact Philips for guidance.
Product
Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0602-2026·2026-04-01
Bulk Colustrum Powder Missing Milk Allergen Declaration
Herbal Creations USA is recalling bulk packaged Colustrum Powder because the product label does not declare milk as an allergen ingredient, posing a risk to consumers with milk allergies.
Product
Bulk packaged Colustrum Powder. packaged with generic product label.
Category
Food
Distribution
0 states
HighFDA (Drugs)·D-0403-2026·2026-04-01
Levothyroxine Sodium Tablets Recalled Nationwide for Subpotent Content
Macleods Pharma USA is recalling Levothyroxine Sodium Tablets nationwide because the medication is subpotent—containing less active ingredient than labeled. The recall includes 1315 bottles.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0402-2026·2026-04-01
FDA Recalls CUROSURF Injectable Drug Over Sterility Assurance Concerns
Chiesi USA, Inc. is recalling 7,235 vials of CUROSURF (poractant alfa) nationwide due to lack of assurance of sterility. The affected intratracheal injection is used in neonatal care.
Product
CUROSURF — CUROSURF (PORACTANT ALFA)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1629-2026·2026-04-01
Orthalign Drill Plate Recalled for Out-of-Specification Manufacturing Defect
Orthalign, Inc. is recalling drill plates used in the Lantern Knee System due to manufacturing defects that can result in excessive bone cuts during surgery. Seven units were distributed in Utah.
Product
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5 REF:402566 component Lantern Knee System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1630-2026·2026-04-01
Orthalign Drill Plate Lantern Knee System Recalled for Out-of-Specification Defect
Orthalign, Inc is recalling Drill Plate components for the Lantern Knee System due to manufacturing defects that can cause excessive bone cuts during orthopedic surgery.
Product
Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7 REF:402567 component Lantern Knee System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1606-2026·2026-04-01
Surgical Compression Screws Recalled for Higher MRI-Induced Heating Than Documented
I.T.S. GmbH is recalling 623 units of HCS Headless Compression Screws nationwide due to RF-induced temperature increases during MRI procedures that exceed what was documented in the product instructions.
Product
HCS - Headless Compression Screw System, Headless Compression Screw, Cannulated; Article Numbers: 31207-10, 31207-12, 31207-14, 31207-16, 31207-18, 31207-20, 31207-24, 31207-26, 31207-28, 31207-30, 31257-12, 31257-14, 31257-16, 31257-18, 31257-20, 31257-22, 31257-24, 31257-28, 31
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1597-2026·2026-04-01
Olecranon Orthopedic Plates Recalled for Updated MRI Safety Information
I.T.S. GmbH is recalling Olecranon orthopedic plates due to updated MRI safety testing revealing higher radiofrequency-induced temperature increases than previously documented. Patients with these implants should consult their doctor before undergoing MRI procedures.
Product
Olecranonplate with Angular Stability with the below descriptions and corresponding article numbers. 1. Olecranon Hook Plate; Article Numbers: 21112-7, 21114-5, 21113-9. 2. Olecranon Plate; Article Numbers: 21111-6, 21111-8, 21111-12.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1599-2026·2026-04-01
Orthopedic screws recalled due to underestimated MRI heating risks
The FDA has recalled I.T.S. surgical screws and washers after testing revealed they heat more during MRI procedures than their instructions indicated. This underdisclosed heating risk could potentially cause tissue damage in patients with these implants.
Product
I.T.S. Screw System with the below descriptions and corresponding article numbers. 1. Cancellous Screw, Cannulated; Article Numbers: 31404-16, 31404-18, 31404-20, 31404-22, 31404-24, 31404-26, 31404-28, 31404-30, 31404-32, 31404-34, 31404-36, 31404-38, 31404-40, 31404-42, 314
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1607-2026·2026-04-01
HLS Hand Locking Plates System MRI Safety Documentation Update Required
The HLS Hand Locking Plates System surgical implants produced higher MRI-related heating than documented in instructions. Updated safety testing revealed increased RF-induced temperature risks requiring updated patient safety guidance.
Product
HLS - Hand Locking Plates System with the below descriptions and corresponding article numbers. 1. Cortical Screw; Article Numbers: 32151-6, 32151-8, 32151-9, 32151-10, 32151-11, 32151-12, 32151-13, 32151-14, 32151-15, 32151-16, 32151-18, 32151-20. 2. HLS Plate, 2 T-Shape
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1602-2026·2026-04-01
Distal humeral plates recalled due to inaccurate MRI safety information
I.T.S. GmbH is recalling 12,059 distal humeral plates because updated MRI testing revealed higher radiofrequency-induced temperature increases than documented in the instructions. Patients with these implants who undergo MRI may experience unexpected heating.
Product
Distal Humeral Plates with Angular Stability with the below descriptions and corresponding article numbers. 1. Cortical Screw, Locking; Article Numbers: 37351-10-N, 37351-12-N, 37351-14-N, 37351-16-N, 37351-18-N, 37351-20-N, 37351-22-N, 37351-24-N, 37351-26-N, 37351-28-N, 373
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1610-2026·2026-04-01
Olympus Endoscope Suction Valve recalled for reprocessor incompatibility
Olympus Corporation is recalling the MAJ-1443 endoscope suction valve because it is no longer compatible with OER-Pro and OER-Elite automated endoscope reprocessors. Improper reprocessing could compromise sterilization of medical equipment.
Product
Olympus Endoscope Suction Valve - MAJ-1443. Model Number: MAJ-1443.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1598-2026·2026-04-01
Orthopedic plates recalled for higher MRI heating than documented
I.T.S. Straight Plates with Angular Stability are recalled because updated MRI safety testing shows higher radiofrequency-induced temperature increases than documented in the Instructions for Use.
Product
I.T.S. Straight Plate with Angular Stability with the below descriptions and corresponding article numbers. 1. Forearm Plate, Curved; Article Numbers: 21604-6, 21604-9. 2. Forearm Plate, Straight; Article Numbers: 21605-11, 21605-6, 21605-9. 3. Straight Compression Pla
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1590-2026·2026-04-01
CT-Navigation System may display inaccurate needle positioning guidance
GE Medical Systems is recalling 125 units of the Imactis CT-Navigation System because the displayed needle position may not match the actual needle trajectory during CT-guided procedures.
Product
Imactis CT-Navigation System, stereotaxic accessory for Computer Tomography (CT), systems, Model Numbers E85101LA and E85101LP
Category
Medical Device
Distribution
Distributed nationwide

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