FoodMay 20, 2026
Dakota Honey Company Original recall — FDA H-0768-2026
Foreign object (stainless steel dust/flakes or shreds of plastic)
Class IIFDA: OngoingDakota Honey Company
Latest records
Latest recalls — page 62
The newest recall records with useful source details are listed here.
FoodMay 20, 2026
Dakota Honey Company Cinnamon-Infused recall — FDA H-0769-2026
Foreign object (stainless steel dust/flakes or shreds of plastic)
Class IIFDA: OngoingDakota Honey Company
FoodMay 20, 2026
Prospector Popcorn brand Belgian Chocolate Toffee flavored recall — FDA H-0779-2026
Products contain undeclared soy, specifically soy lecithin.
Class IIFDA: OngoingProspector Popcorn, LLC
FoodMay 20, 2026
Sugar Foods Kroger HOMESTYLE Cheese AND Garlic CROUTONS NET WT 5 OZ recall — FDA H-0781-2026
Possible Salmonella in croutons. The firm was notified by their supplier that the non-fat milk powder used to manufacture the product was recalled due to possible salmonella.
Class IFDA: CompletedSugar Foods LLC
FoodMay 20, 2026
Ferris Coffee and Nut Company Frederik's by meijer Vanilla Bourbon Trail Mix, packed in recall — FDA H-0774-2026
Undeclared allergens (wheat and soy).
Class IIFDA: TerminatedFerris Coffee and Nut Company, Inc.
FoodMay 20, 2026
Pure Ground Ingredients-Organic Peppermint Leaf Powder recall — FDA H-0853-2026
Product has the potential to be contaminated with Salmonella.
Class IFDA: TerminatedPure Ground Ingredients, Inc.
FoodMay 20, 2026
Dakota Honey Company the Honey Flight recall — FDA H-0772-2026
Foreign object (stainless steel dust/flakes or shreds of plastic)
Class IIFDA: OngoingDakota Honey Company
FoodMay 20, 2026
Dakota Honey Company Jalapeno recall — FDA H-0771-2026
Foreign object (stainless steel dust/flakes or shreds of plastic)
Class IIFDA: OngoingDakota Honey Company
FoodMay 20, 2026
WE R NUTS Uncle Giuseppe's Marketplace Milk Chocolate Bridge Mix, 11 oz recall — FDA H-0775-2026
Contains undeclared allergens (cashews, milk, and soy).
Class IIFDA: OngoingWE R NUTS
FoodMay 20, 2026
Dakota Honey Company Salted Caramel recall — FDA H-0770-2026
Foreign object (stainless steel dust/flakes or shreds of plastic)
Class IIFDA: OngoingDakota Honey Company
VehicleMay 19, 2026
Model Y labels recall — NHTSA campaign 26V315000
Tesla, Inc. (Tesla) is recalling certain 2025-2026 Model Y vehicles. The certification label may not have been installed. As such, these vehicles fail to comply with the requirements of 49…
labelsTesla, Inc.
VehicleMay 19, 2026
Hyundai Motor automatic emergency braking recall — NHTSA campaign 26V316000
Hyundai Motor America (Hyundai) is recalling certain 2025-2026 Santa Cruz, Tucson, Tucson Hybrid, and Tucson Plug-In Hybrid Electric (PHEV) vehicles. Software in the front cameras may cause…
automatic emergency brakingHyundai Motor America
VehicleMay 14, 2026
General Motors hub recall — NHTSA campaign 26V304000
General Motors, LLC is recalling certain 2025–2026 Cadillac Escalade, Escalade ESV, Chevrolet Suburban 1500, Tahoe, GMC Yukon, and Yukon XL vehicles with 24-inch wheels. Incorrect bolts may…
hubGeneral Motors, LLC
Medical DeviceMay 13, 2026
Cook Beacon Tip Centimeter Sizing Catheter RPN/GPN NR5.0-35-70-P-10S-0-CSC-20 G31213 recall — FDA Z-1936-2026
Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated with device…
Class IFDA: OngoingCook Incorporated
Medical DeviceMay 13, 2026
Medline Convenience Kits: 1) CHEST TUBE INSERTION TRAY recall — FDA Z-2106-2026
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceMay 13, 2026
Mint Lesion; Software Versions: 3.4.0 up to 3.9.5 recall — FDA Z-2068-2026
If the connection between a mint Lesion workstation and the mint Lesion server is interrupted while performing a read, in rare cases some information may be lost or incorrectly linked to…
Class IIFDA: OngoingMint Medical GmbH
Medical DeviceMay 13, 2026
Cook Aurous Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20-01 GPN G47308 Sizing recall — FDA Z-1935-2026
Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated with device…
Class IFDA: OngoingCook Incorporated
Medical DeviceMay 13, 2026
Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06 recall — FDA Z-1855-2026
Reloads for curved-tipped stapler may potentially produce an incomplete staple line.
Class IFDA: OngoingIntuitive Surgical, Inc.
Medical DeviceMay 13, 2026
Medline Convenience Kits: 1) KIT TRIPLE LUMEN INSERTION recall — FDA Z-2123-2026
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceMay 13, 2026
Cook Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20 GPN G11916 Catheters for recall — FDA Z-1934-2026
Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated with device…
Class IFDA: OngoingCook Incorporated
Medical DeviceMay 13, 2026
Erbe Medical ERBEFLO 2, Endoscopy Pump Tubing/Cap Set, REF: 20325-222 recall — FDA Z-2064-2026
Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible to unintended water flow from…
Class IIFDA: OngoingErbe Medical, LLC
Medical DeviceMay 13, 2026
Erbe Medical ERBEFLO CleverCap: Hybrid Tubing/Cap Set for Olympus Scopes, 20325-201 recall — FDA Z-2063-2026
Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible to unintended water flow from…
Class IIFDA: OngoingErbe Medical, LLC
Medical DeviceMay 13, 2026
Medline Industries See RES for complete list recall — FDA Z-2114-2026
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging…
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceMay 13, 2026
AVID Medical Halyard PERC TRAY kit recall — FDA Z-1977-2026
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Class IFDA: OngoingAVID Medical, Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
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 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categories