Agency

U.S. Food and Drug Administration

The FDA regulates food, drugs, biologics, medical devices, and tobacco. We aggregate Class I, II, and III enforcement actions across its three recall streams.

Visit the official FDA site →

976–1000 of 26417

HighFDA (Food)·H-0596-2026·2026-04-01
Ajinomoto Ling Ling Fried Rice Recalled for Glass Contamination
Ajinomoto Foods North America is recalling Item 81097 Ling Ling Restaurant Style Fried Rice due to glass fragments measuring 1-3 cm long and 2-4 mm wide found in the product. Affected units with Best By dates 9/21/2026 through 3/8/2027 were distributed across 40 U.S. states.
Product
Item 81097 Ajinomoto Ling Ling Restaurant Style Fried Rice Savory Vegetable - A Chinese Style Fried Rice with Edamame, Carrots, Fire Roasted Corn & Red Bell Peppers Prepared with Sweet Soy Sauce Infused Rice. Net wt. 17oz. Retail box UPC 010878810915. Product packaging is flexib
Category
Food
Distribution
43 states
HighFDA (Food)·H-0622-2026·2026-04-01
Rose and Shore Margarita Thin Crust Pizza Recalled for Metal Contamination
Rose and Shore, Inc. is recalling 14" Margarita Thin Crust Pizza due to potential metal pieces found in the tomato ingredient. The product was distributed to retail locations in California, Oregon, Arizona, Idaho, and Texas.
Product
14" Margarita Thin Crust Pizza; 8 units per case. Keep Frozen UPC code: 1713940060
Category
Food
Distribution
0 states
HighFDA (Food)·H-0600-2026·2026-04-01
Ajinomoto Vegetable Gyoza Dumplings recalled for glass fragments
Ajinomoto Foods North America Inc. is recalling Vegetable Gyoza Dumplings (UPC 071757055483) due to the presence of glass fragments in the product, which could pose a choking or injury hazard if ingested.
Product
Item 6430143 Ajinomoto Vegetable Gyoza Dumplings 12ct. Net wt. 8.92oz. per package. Retail package UPC: 071757055483. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 20/8.92oz. packages or 11.15 lbs. per case. Carton UP
Category
Food
Distribution
43 states
HighFDA (Food)·H-0597-2026·2026-04-01
Ajinomoto Tai Pei Shrimp Fried Rice Recalled for Glass Contamination
Ajinomoto Foods North America Inc. is recalling Tai Pei Shrimp Fried Rice due to glass fragments found in the product. Glass pieces measuring 1–3 cm long and 2–4 mm wide pose a choking and injury risk.
Product
Item 81146 Ajinomoto Tai Pei Shrimp Fried Rice - Shrimp, vegetables & fried rice with oyster flavored sauce. Net wt. 48oz or 3lbs. per box. Retail box UPC 070077811465. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 4
Category
Food
Distribution
43 states
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
HighFDA (Devices)·Z-1613-2026·2026-04-01
Olympus OER-Pro endoscope reprocessor incompatible with MAJ accessories
Olympus Corporation of the Americas is recalling 3,354 units of the OER-Pro endoscope reprocessor because MAJ-1443 and MAJ-1444 accessories are no longer compatible with it.
Product
Olympus Endoscope Reprocessor OER-Pro. Model Number: N3058140.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1640-2026·2026-04-01
Olympus PK Cutting Forceps recalled due to defective welds
Olympus is recalling 444 units of the PK Cutting Forceps (Model PK-CF0533) worldwide because defective welds in supplier-provided components can cause the instrument's jaw to break during surgical use.
Product
Brand Name: Olympus PK Cutting Forceps, 5mm 33cm Product Name: PK Cutting Forceps Model/Catalog Number: PK-CF0533 Product Description: An assembly of devices intended to generate and apply radio-frequency (RF) alternating current to soft tissues for cutting and coagulation dur
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0629-2026·2026-04-01
Tops GOLD Green Chilli Pickle recalled for potential erucic acid
Tops GOLD Green Chilli Pickle, 31.74 oz cans, is recalled due to potential adulteration with erucic acid from mustard oil. The product was distributed in CA, NV, OR, UT, and WA.
Product
Tops GOLD Green Chilli Pickle NET QTY.: 31.74oz PRODUCT OF INDIA UPC: 8904288612837 INGREDIENTS:***Mustard Oil***
Category
Food
Distribution
5 states
HighFDA (Food)·H-0608-2026·2026-04-01
King Harvest Black Olive Hummus recall due to aluminum pieces
Pacific Coast Fresh CO is recalling King Harvest brand Black Olive Hummus because it may contain aluminum pieces. The product was distributed in Oregon and Washington.
Product
King Harvest brand Black Olive Hummus. Product is packed in 10oz plastic tubs with a clear film seal and a lid. Keep Refrigerated - Handcrafted in Portland OR kingharvesthummus.com. Black Olive Hummus 10 oz. UPC 025726 311216
Category
Food
Distribution
2 states
HighFDA (Food)·H-0595-2026·2026-04-01
Ajinomoto Golden Tiger Vegetable Fried Rice recalled for glass fragments
Ajinomoto Foods North America Inc. is recalling Ajinomoto Golden Tiger Vegetable Fried Rice due to the presence of glass fragments varying from 1–3 cm long and 2–4 mm wide in the product.
Product
Item 5654390 Ajinomoto Golden Tiger Vegetable Fried Rice - Long grain white rice and crispy vegetables in a savory sauce. Net wt. 3lbs per bag. Retail bag UPC 076366565439. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There ar
Category
Food
Distribution
43 states
HighFDA (Food)·H-0589-2026·2026-04-01
Chilli Spanish Peanuts First Street recalled for glass contamination
Western Mixers Produce & Nuts, Inc. is recalling First Street Chilli Spanish Peanuts (11 oz) because glass fragments were found in sealed containers. Affected lots have expiration dates of 2/11/2027, 2/13/2027, and 2/23/2027.
Product
Chilli Spanish Peanuts, First Street brand, 11oz clear plastic container. UPC: None Item Code: 2608-T20
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0594-2026·2026-04-01
Ajinomoto Japanese-Style Vegetable Fried Rice Recalled for Glass Contamination
Ajinomoto Foods North America Inc. is recalling Item 5650893 Japanese-Style Vegetable Fried Rice because some packages may contain glass fragments measuring 1–3 cm long and 2–4 mm wide.
Product
Item 5650893 Ajinomoto Japanese-Style Vegetable Fried Rice made with hijiki seaweed, fried tofu, edamame, and other colorful vegetables in an umami dashi sauce Net wt. 17oz. Retail box UPC 071757508934. Product packaging is flexible bags in a master case or flexible bags in cart
Category
Food
Distribution
43 states
HighFDA (Food)·H-0648-2026·2026-04-01
Gorditas de Azucar recalled for missing wheat and soy allergen labels
Distribuidora de Alimentos Sendero LLC is recalling Gorditas de Azucar (UPC 860010238134) distributed in Texas because the product labels do not disclose wheat and soy allergens.
Product
Gorditas de Azucar UPC 860010238134
Category
Food
Distribution
0 states
HighFDA (Food)·H-0627-2026·2026-04-01
Tops GOLD Khatta Meetha Pickle recalled for potential erucic acid contamination
Mangalm LLC is recalling Tops GOLD Khatta Meetha Pickle due to potential adulteration with erucic acid from the mustard oil ingredient. The 33.51 oz cans were distributed in California, Nevada, Oregon, Utah, and Washington.
Product
Tops GOLD Khatta Meetha Pickle NET QTY.: 33.51oz PRODUCT OF INDIA UPC: 8904288611427 INGREDIENTS:***Mustard Oil***
Category
Food
Distribution
5 states
HighFDA (Food)·H-0606-2026·2026-04-01
King Harvest Sundried Tomato Hummus recalled for aluminum pieces
Pacific Coast Fresh CO is recalling King Harvest brand Sundried Tomato Hummus due to the potential presence of aluminum pieces in the product.
Product
King Harvest brand Sundried Tomato Hummus. Product is packed in 10oz plastic tubs with a clear film seal and a lid. Keep Refrigerated - Handcrafted in Portland OR kingharvesthummus.com. Sundried Tomato Hummus 10 oz. UPC 025726 311186.
Category
Food
Distribution
2 states
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