FoodJan 14, 2026
DIRECT SOURCE SEAFOOD MARKET 32 by Price Chopper brand, frozen RAW SHRIMP easy peel recall — FDA H-0380-2026
Shrimp may be contaminated with Cesium-137 (Cs-137).
Class IIFDA: TerminatedDIRECT SOURCE SEAFOOD LLC
Monthly breakdown
2026 recalls by month
Select a month to review the recall records reported during that period.
September 2026300 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categories
2026 recalls — page 118
Records are ordered by the best available source date.
FoodJan 14, 2026
Rovira Biscuit Net Wt recall — FDA H-0358-2026
Undeclared colors FD&C Yellow #6, and FD&C Red 40
Class IIFDA: TerminatedRovira Biscuit Corporation
FoodJan 14, 2026
Rovira Biscuit Vanilla Treats Crackers, Rovira, Net Wt recall — FDA H-0361-2026
Undeclared colors FD&C Yellow #6, and FD&C Red 40
Class IIFDA: TerminatedRovira Biscuit Corporation
FoodJan 14, 2026
Sam Dry Fruits and Nuts Enterprises Sam Dry Fruits & Nuts PISTACHIO Meats Whole LOT # recall — FDA H-0357-2026
Potential contamination with Salmonella.
Class IFDA: OngoingSam Dry Fruits and Nuts Enterprises, Inc
FoodJan 14, 2026
Rovira Biscuit Tempting Crackers Tray, Rovira, 3 foil wrap trays per Net Wt recall — FDA H-0359-2026
Undeclared colors FD&C Yellow #6, and FD&C Red 40
Class IIFDA: TerminatedRovira Biscuit Corporation
FoodJan 14, 2026
Meijer 128 FL OZ recall — FDA H-0408-2026
Floating black foreign substance in the product
Class IIFDA: TerminatedMeijer Inc
FoodJan 14, 2026
Fresh & Ready Foods Spicy Egg Potatoes Cheese Tacos, Fresh to You brand, Ready to recall — FDA H-0355-2026
Foreign material.
Class IIFDA: TerminatedFresh & Ready Foods LLC
FoodJan 14, 2026
DIRECT SOURCE SEAFOOD waterfront BISTRO brand Frozen Raw Shrimp EZ PEEL SHELL & TAIL recall — FDA H-0379-2026
Shrimp may be contaminated with Cesium-137 (Cs-137).
Class IIFDA: TerminatedDIRECT SOURCE SEAFOOD LLC
FoodJan 14, 2026
McCain Foods USA Ore-Ida Tater Tots shaped potatoes, item number OIF00215A recall — FDA H-0375-2026
Clear hard plastic fragments.
Class IIFDA: TerminatedMcCain Foods USA Inc
FoodJan 14, 2026
Fresh & Ready Foods Spicy Veggie Breakfast Burrito, Fresh to You, Ready to Eat recall — FDA H-0353-2026
Foreign material.
Class IIFDA: TerminatedFresh & Ready Foods LLC
FoodJan 14, 2026
Town Food Service EQ CO Inc recall — FDA H-0351-2026
Product found to contain leachable lead levels.
Class IIFDA: OngoingTown Food Service Equip Co Inc
FoodJan 14, 2026
Fresh & Ready Foods Spicy Breakfast Burrito, Sprig & Sprout brand, Ready to Eat recall — FDA H-0354-2026
Foreign material.
Class IIFDA: TerminatedFresh & Ready Foods LLC
FoodJan 14, 2026
McCain Foods USA Sysco Imperial Potato Tater Barrel, item number 1000006067 recall — FDA H-0376-2026
Clear hard plastic fragments.
Class IIFDA: TerminatedMcCain Foods USA Inc
FoodJan 14, 2026
Rovira Biscuit Vanilla Econo, Galletas de Vainilla, 8 paquets per Net Wt recall — FDA H-0360-2026
Undeclared colors FD&C Yellow #6, and FD&C Red 40
Class IIFDA: TerminatedRovira Biscuit Corporation
DrugJan 14, 2026
Fesoterodine Fumarate, Extended-release Tablets, 8 mg, 30 Tablets recall — FDA D-0248-2026
Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.
Class IIIFDA: OngoingAlembic Pharmaceuticals Limited
DrugJan 14, 2026
Oxycodone and Acetaminophen CII Tablets USP, 7.5 mg/325 mg, 100 tablets recall — FDA D-0255-2026
Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets.
Class IIFDA: OngoingSpecGx, LLC
DrugJan 14, 2026
ReBoost Nasal Spray, 0.68 fl. oz. (20 mL) bottles recall — FDA D-0288-2026
Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
Class IFDA: OngoingMedinatura New Mexico, inc.
DrugJan 14, 2026
ClearLife Allergy Nasal Spray, Extra Strength, 0.68 fl. oz. (20 mL) bottles recall — FDA D-0289-2026
Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter.
Class IFDA: OngoingMedinatura New Mexico, inc.
Medical DeviceJan 7, 2026
Sheathing Technologies Sheathes3D Seamless Viral Barrier, Latex-Free, 7/8"D Tapered to 2.9"W recall — FDA Z-1006-2026
Vaginal/rectal ultrasound probe covers with a viral barrier may have product defects, which may result in contamination during use, posing an infection risk.
Class IIFDA: OngoingSheathing Technologies Inc.
Medical DeviceJan 7, 2026
Mastisol Liquid Adhesive Liquid Adhesive recall — FDA Z-1005-2026
Butyrate tube cracks during actuation, rendering product unusable.
Class IIFDA: OngoingFerndale Laboratories, Inc.
Medical DeviceJan 7, 2026
Philips EPIQ Ultrasound Systems (various models) used in conjunction with the X5-1c recall — FDA Z-1007-2026
Retroactive: Ultrasound may experience an unexpected automatic reboot, resulting in damage to transducer.
Class IIFDA: CompletedPhilips Ultrasound, LLC
Medical DeviceJan 7, 2026
Beaver-Visitec International BVI Leos Laser and Endoscopy System recall — FDA Z-1008-2026
Manufacturing deviation in which the ferrites specified for the USB cable assembly linking the Nurse Monitor touchscreen to the System Controller were not installed as intended. The…
Class IIFDA: OngoingBeaver-Visitec International, Inc.
DrugJan 7, 2026
Novo Nordisk Wegovy (semaglutide) Injection, 0.5 mg/0.5 mL, 4 Single-Dose Prefilled Pens recall — FDA D-0244-2026
Presence of Particulate Matter: Hair was found in a prefilled syringe
Class IIFDA: OngoingNovo Nordisk Inc.
DrugJan 7, 2026
Novo Nordisk Wegovy (semaglutide) Injection, 1 mg/0.5 mL, 4 Single-Dose Prefilled Pens recall — FDA D-0245-2026
Presence of Particulate Matter: Hair was found in a prefilled syringe
Class IIFDA: OngoingNovo Nordisk Inc.
About the 2026 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.