FoodMay 27, 2026
GHIRARDELLI SWEET GROUND POWDER CHOCOLATE & COCOA NET WT 48oz recall — FDA H-0845-2026
Potential contamination with Salmonella.
Class IFDA: OngoingGhirardelli Chocolate Company
Latest records
Latest recalls — page 40
The newest recall records with useful source details are listed here.
FoodMay 27, 2026
GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX WHITE MOCHA NET WT recall — FDA H-0840-2026
Potential contamination with Salmonella.
Class IFDA: OngoingGhirardelli Chocolate Company
FoodMay 27, 2026
Pork King Good Onion & Sour Cream Seasoning recall — FDA H-0830-2026
Seasoning was made with recalled California Dairies milk powder due to Salmonella contamination.
Class IFDA: CompletedPork King Good, LLC
FoodMay 27, 2026
Wellnov Supplements Liposomal Kids Liquid Multivitamin Drops recall — FDA H-0802-2026
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Class IIFDA: TerminatedWellnov Supplements LLC
FoodMay 27, 2026
GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX FROZEN HOT COCOA NET recall — FDA H-0838-2026
Potential contamination with Salmonella.
Class IFDA: OngoingGhirardelli Chocolate Company
FoodMay 27, 2026
Wellnov Supplements Liposomal B12 Spray recall — FDA H-0807-2026
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Class IIFDA: TerminatedWellnov Supplements LLC
FoodMay 27, 2026
PS Seasoning & Spices Blackstone Parmesan Ranch Seasoning, Net Wt 7.3 oz recall — FDA H-0817-2026
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Class IFDA: OngoingPS Seasoning & Spices, Inc.
FoodMay 27, 2026
Wellnov Supplements Liposomal Sleep Spray recall — FDA H-0808-2026
Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.
Class IIFDA: TerminatedWellnov Supplements LLC
FoodMay 27, 2026
Fontana Flavors VG7274D1 Natural Cream of Mushroom Type Flavor, Net Weight: 50 recall — FDA H-0812-2026
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Class IFDA: TerminatedFontana Flavors, Inc
FoodMay 27, 2026
GHIRARDELLI SWEET GROUND POWDER WHITE CHOCOLATE FLAVORED NET recall — FDA H-0844-2026
Potential contamination with Salmonella.
Class IFDA: OngoingGhirardelli Chocolate Company
FoodMay 27, 2026
PS Seasoning & Spices Ellsworth Sour Cream + Onion Seasoning, Part #: 180000113 recall — FDA H-0814-2026
Product was made with milk powder recalled by the supplier due to Salmonella contamination.
Class IFDA: OngoingPS Seasoning & Spices, Inc.
VehicleMay 21, 2026
Chrysler camera recall — NHTSA campaign 26V327000
Chrysler (FCA US, LLC) is recalling certain 2019 and 2023 Chrysler Pacifica, 2024 Ram 1500, Ram 2500, and 2024-2025 Jeep Wrangler vehicles. Contamination in the central vision processing…
cameraChrysler (FCA US, LLC)
VehicleMay 21, 2026
Honda front passenger recall — NHTSA campaign 26V332000
Honda (American Honda Motor Co.) is recalling certain 2018-2021, 2023 Acura TLX, 2019-2024 RDX, 2017-2020, 2022-2026 MDX, 2017-2021, 2023, 2025 Honda Ridgeline, 2017-2022 Pilot, 2019-2021…
front passengerHonda (American Honda Motor Co.)
VehicleMay 21, 2026
Chrysler air bag control module software recall — NHTSA campaign 26V328000
Chrysler (FCA US, LLC) is recalling certain 2022-2026 Jeep Grand Cherokee and 2023-2025 Jeep Grand Cherokee L vehicles. A software error in the occupant restraint controller module may…
air bag control module softwareChrysler (FCA US, LLC)
Medical DeviceMay 20, 2026
Medline medical convenience kits, containing Namic Manifold, Labeled as: 1 recall — FDA Z-2147-2026
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Class IFDA: OngoingMedline Industries, LP
Medical DeviceMay 20, 2026
Medline Industries Namic Preceptor Manifold, custom, Medline Product Number/SKU 64039307 recall — FDA Z-2142-2026
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Class IFDA: OngoingMedline Industries, LP
Medical DeviceMay 20, 2026
Medline Industries Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038402 recall — FDA Z-2140-2026
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Class IFDA: OngoingMedline Industries, LP
Medical DeviceMay 20, 2026
GE Medical Systems Revolution CT, x-ray computed tomography, Model Numbers 5590000 and recall — FDA Z-2150-2026
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain…
Class IIFDA: OngoingGE Medical Systems, LLC
Medical DeviceMay 20, 2026
DONJOY ICEMAN, W/COLDPAD, NS, RH recall — FDA Z-2137-2026
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Class IIFDA: OngoingDJO, LLC
Medical DeviceMay 20, 2026
Medline Industries Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038200 recall — FDA Z-2138-2026
Medline has identified the presence of particulate within the fluid path of the Manifolds.
Class IFDA: OngoingMedline Industries, LP
Medical DeviceMay 20, 2026
Jolife AB LUCAS 2 recall — FDA Z-2161-2026
Due to a subset of chest compression systems/devices where the service performed on the systems were not appropriately documented (The documents for the service performed to justify the…
Class IIFDA: OngoingJolife AB
Medical DeviceMay 20, 2026
Integra LifeSciences Codman CerebroFlo EVD Catheter with Endexo Technology recall — FDA Z-2173-2026
Out-of-specification endotoxin result that did not meet the acceptance criteria.
Class IIFDA: OngoingIntegra LifeSciences Corp. (NeuroSciences)
Medical DeviceMay 20, 2026
GE Medical Systems Revolution Apex Plus, X-ray Computed Tomography, Model Number 5590000-25 recall — FDA Z-2152-2026
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain…
Class IIFDA: OngoingGE Medical Systems, LLC
Medical DeviceMay 20, 2026
DONJOY ICEMAN W/,UNIV,LOOP,NS,RH recall — FDA Z-2135-2026
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Class IIFDA: OngoingDJO, LLC
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
August 2026145 records · 4 categoriesJuly 2026367 records · 4 categoriesJune 2026371 records · 4 categoriesMay 2026329 records · 4 categoriesApril 2026406 records · 4 categoriesMarch 2026171 records · 4 categoriesFebruary 2026121 records · 4 categoriesJanuary 202663 records · 3 categoriesDecember 2025101 records · 3 categoriesNovember 202596 records · 3 categoriesOctober 2025134 records · 3 categoriesSeptember 2025116 records · 3 categories