FoodApr 1, 2026
Pacific Coast Fresh CO King Harvest brand Roasted Red Pepper Hummus recall — FDA H-0605-2026
Foreign material (aluminum pieces).
Class IIFDA: TerminatedPacific Coast Fresh CO
Latest records
Latest recalls — page 68
The newest recall records with useful source details are listed here.
FoodApr 1, 2026
American Laboratories Pepsin 1:3000 Powder, 50 kg, Item #FTI-G0193-00, American recall — FDA H-0612-2026
Potential Salmonella contamination.
Class IIFDA: TerminatedAmerican Laboratories, LLC
FoodApr 1, 2026
Albertsons Companies Lucerne 2% Cottage Cheese 2% Milkfat Small Curd Vitamin A recall — FDA H-0630-2026
Metal fragments. The potential foreign object is a hard, metal (stainless steel), curled spring. Dimensions of a similar spring measure 2.27mm in cross-sectional thickness and 25.38mm in…
Class IIFDA: TerminatedAlbertsons Companies LLC
FoodApr 1, 2026
Mangalm Tops GOLD Mixed Pickle NET QTY.: 31.74oz PRODUCT OF INDIA UPC recall — FDA H-0624-2026
Potential adulteration with erucic acid from mustard oil ingredient.
Class IIFDA: OngoingMangalm LLC
FoodApr 1, 2026
Lidl US TRADING Favorina Chocolate Ladybugs German-Style Nougat, Net Wt 3.52 recall — FDA H-0631-2026
Label does not specify type of tree nut contained in the product.
Class IIFDA: OngoingLidl US TRADING
FoodApr 1, 2026
Ajinomoto Foods Item 5650233 Trader Joe's Vegetable Fried Rice, net wt recall — FDA H-0592-2026
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
Class IIFDA: OngoingAjinomoto Foods North America Inc.
FoodApr 1, 2026
Ajinomoto Foods vegetables & fried rice with oyster flavored sauce recall — FDA H-0597-2026
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
Class IIFDA: OngoingAjinomoto Foods North America Inc.
FoodApr 1, 2026
SiluetaYa Mexican Tejocote Roots Supplement Pieces recall — FDA H-0647-2026
Product contains yellow oleander
Class IFDA: OngoingSiluetaya, LLC
FoodApr 1, 2026
Ajinomoto Foods Item 6430143 Ajinomoto Vegetable Gyoza Dumplings 12ct recall — FDA H-0600-2026
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
Class IIFDA: OngoingAjinomoto Foods North America Inc.
FoodApr 1, 2026
Rose and Shore 14" Margarita Thin Crust Pizza recall — FDA H-0622-2026
potential foreign object (metal pieces) in ingredient (Tomatoes)
Class IIFDA: TerminatedRose and Shore, Inc.
FoodApr 1, 2026
Ajinomoto Foods Item 81097 Ajinomoto Ling Ling Restaurant Style Fried Rice recall — FDA H-0596-2026
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
Class IIFDA: OngoingAjinomoto Foods North America Inc.
FoodApr 1, 2026
Ajinomoto Foods Item 6430093 Ajinomoto Green Gyoza Vegetable & Edamame recall — FDA H-0599-2026
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
Class IIFDA: OngoingAjinomoto Foods North America Inc.
DrugApr 1, 2026
SODIUM IODIDE I-131 Gelatin Capsule Pack for use with the Sodium Iodide I-131 Kit recall — FDA D-0401-2026
Failed Tablet/Capsule Specifications
Class IIIFDA: OngoingRadnostix
DrugApr 1, 2026
Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 30 mg recall — FDA D-0406-2026
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
Class IIFDA: OngoingTeva Pharmaceuticals USA, Inc
DrugApr 1, 2026
Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 10 mg recall — FDA D-0404-2026
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
Class IIFDA: OngoingTeva Pharmaceuticals USA, Inc
DrugApr 1, 2026
Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 20 mg recall — FDA D-0405-2026
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
Class IIFDA: OngoingTeva Pharmaceuticals USA, Inc
VehicleMar 31, 2026
Ford hard parts internal/mechanical recall — NHTSA campaign 26V205000
Ford Motor Company (Ford) is recalling certain 2026 Explorer and Mustang vehicles. The engine piston circlips may have been incorrectly installed during manufacturing, which can result in…
hard parts internal/mechanicalFord Motor Company
VehicleMar 31, 2026
Ford fan/motor recall — NHTSA campaign 26V202000
Ford Motor Company (Ford) is recalling certain 2026 Lincoln Aviator and Explorer vehicles. The heating, ventilation and air-conditioning (HVAC) system may fail, which can cause the…
fan/motorFord Motor Company
Medical DeviceMar 25, 2026
GE Medical Systems Centricity Universal Viewer Software Versions 7.0 through 7.0 Sp2.0.1, a recall — FDA Z-1569-2026
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which…
Class IIFDA: OngoingGE Medical Systems, LLC
Medical DeviceMar 25, 2026
Welch Allyn Spot Vision Screener VS100 recall — FDA Z-1573-2026
Display screen may unintentionally flicker due to a software issue. Exposure to flickering lights may induce photosensitive seizure activity in susceptible individuals.
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceMar 25, 2026
Abbott Diagnostics Scarborough ID NOW" Influenza A & B 2 recall — FDA Z-1565-2026
It was confirmed that the impacted lot has a higher occurrence of invalid rates when compared to the product Instructions for Use.
Class IIFDA: OngoingAbbott Diagnostics Scarborough, Inc.
Medical DeviceMar 25, 2026
GE Medical Systems Centricity Universal Viewer Software Versions 5.0 SP6 through UV 5.0 recall — FDA Z-1571-2026
There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which…
Class IIFDA: OngoingGE Medical Systems, LLC
Medical DeviceMar 25, 2026
Aptima HPV Assay recall — FDA Z-1586-2026
Due to product exhibiting potential to generate either invalid or false negative results.
Class IIFDA: OngoingHologic, Inc.
Medical DeviceMar 25, 2026
STA Liatest D-Di recall — FDA Z-1585-2026
After receiving customer complaints, investigations confirmed the presence of a positive bias in D-Dimer measurements throughout the entire analytical range.
Class IIFDA: OngoingDiagnostica Stago, Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
August 2026145 records · 4 categoriesJuly 2026369 records · 4 categoriesJune 2026373 records · 4 categoriesMay 2026330 records · 4 categoriesApril 2026407 records · 4 categoriesMarch 2026179 records · 4 categoriesFebruary 2026329 records · 4 categoriesJanuary 2026210 records · 4 categoriesDecember 2025184 records · 4 categoriesNovember 202596 records · 3 categoriesOctober 2025139 records · 3 categoriesSeptember 2025116 records · 3 categories