State

Rhode Island product recalls

73,741 recalls have nationwide distribution and so reach Rhode Island. 3,053 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total: 3,053
Critical: 221
Severe: 707
Most recent: 2026-10-28

Of the 3,053 recalls naming Rhode Island we have scored against our rubric, 221 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 707 (23%) are Severe.

Which agencies issued them

These figures cover only the 3,053 recalls whose distribution notice names Rhode Island specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36301–36325 of 76794

SevereFDA (Drugs)·D-0587-2019·2019-03-20
FDA Recalls King Bio Homeopathic Breast Inflammation Product for Microbial Contamination
King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Breast Inflammations & Discomforts due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.
Product
Dr. King's Natural Medicine Homeopathic Breast Inflammations & Discomforts, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955500322, NDC 57955-5003-2
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0748-2019·2019-03-20
King Bio Recalls Dr. King's SafeCare Rx Fears & Nightmares Due to Microbial Contamination
King Bio Inc. is recalling 96 bottles of Dr. King's SafeCare Rx Fears & Nightmares Mind & Body due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.
Product
Dr. King's SafeCare Rx Fears & Nightmares Mind & Body, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955181026, NDC 57955-1811-2
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0923-2019·2019-03-20
King Bio Inc. Recalls NET Remedies #7 Homeopathic Preparation Due to Microbial Contamination
King Bio Inc. is recalling NET Remedies #7 Homeopathic Preparation, Oral Liquid, 57 mL, due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.
Product
NET Remedies #7 Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0816-2019·2019-03-20
King Bio Recalls Calcium Metabolizer Due to Microbial Contamination
King Bio Inc. is recalling Dr. King's SafeCare Rx Calcium Metabolizer due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.
Product
Dr. King's SafeCare Rx Calcium Metabolizer, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955013129, NDC 57955-0131-2
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0582-2019·2019-03-20
King Bio Homeopathic Leg Cramp Relief Recalled for Microbial Contamination
King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Leg Cramp & Spasm Relief due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.
Product
Dr. King's Natural Medicine Homeopathic Leg Cramp & Spasm Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955543527, NDC 57955-6035-2
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0531-2019·2019-03-20
King Bio Recalls Homeopathic Heart Regularity Due to Microbial Contamination
King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Heart Regularity due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.
Product
Dr. King's Natural Medicine Homeopathic Heart Regularity, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955506522, NDC 57955-5065-2
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0770-2019·2019-03-20
King Bio Recalls Dr. King's SafeCare Rx Candida Due to Microbial Contamination
King Bio Inc. is recalling Dr. King's SafeCare Rx Candida bottles due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.
Product
Dr. King's SafeCare Rx Candida, 8 fl. oz. (236 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955620686, NDC 57955-6207-8
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0609-2019·2019-03-20
King Bio Homeopathic Hair & Nails Formula Recalled for Microbial Contamination
King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Hair & Nails Formula due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.
Product
Dr. King's Natural Medicine Homeopathic Hair & Nails Formula, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955504924, NDC 57955-5049-2
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0950-2019·2019-03-20
King Bio Para Solve Homeopathic Liquid Recalled for Microbial Contamination
King Bio Inc. is recalling NET Remedies #6 Para Solve Homeopathic Preparation due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.
Product
NET Remedies #6 Para Solve Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4206-2
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0732-2019·2019-03-20
King Bio Recalls Anti-Aging Cream Due to Microbial Contamination
King Bio Inc. is recalling Dr. King's SafeCare Rx Anti-Aging & Wrinkles For Men due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.
Product
Dr. King's SafeCare Rx Anti-Aging & Wrinkles For Men, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955714729, NDC 57955-7148-2
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0557-2019·2019-03-20
King Bio Recalls Homeopathic Arnica Due to Microbial Contamination
King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Advanced Arnica due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.
Product
Dr. King's Natural Medicine Homeopathic Advanced Arnica, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955598428, NDC 57955-5984-2
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1006-2019·2019-03-20
FDA Recalls NexGen Trabecular Metal Tibial Augments Due to Labeling Mismatch
Zimmer Trabecular Metal Technology is recalling 26 units of NexGen Trabecular Metal Tibial Half Block Augments because the product in the box may not match the label.
Product
NexGenTrabecular Metal Tibial Half Block Augment, Left Lateral/Right Medial, Size 4 5MM Thickness W/Screws Item Number: 00544800436 Product Usage: The Trabecular Metal Tibial Cone Augments are intended for use where severe degeneration, trauma, or other pathology of the…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·19730·2019-03-20
Kubota Recalls Zero Turn Mowers Due to Fire Hazard
Kubota is recalling about 3,850 zero turn mowers because the throttle cable can contact internal wiring, posing a fire hazard. No injuries have been reported.
Product
Kubota Zero Turn Mowers
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·19V221000·2019-03-20
Osage Ambulances Recalled for Brake Lights Illuminating Without Pedal Press
Osage is recalling 2015-2019 Brave, Warrior, and Super Warrior ambulances because brake lights may illuminate when the brake pedal is not pressed, potentially confusing other drivers.
Product
OSAGE — OSAGE SUPER WARRIOR, BRAVE, WARRIOR
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·19088·2019-03-20
Honda Recalls Portable Generators Due to Fire and Burn Hazards
American Honda is recalling approximately 200,000 portable generators because a fuel valve leak can cause fire and burn hazards. No injuries have been reported.
Product
Honda EU2200i, EU220i Companion and EB2200i Portable Generators
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0994-2019·2019-03-20
Durex Pleasure Pack Condoms Recalled for Burst Pressure Failure
Reckitt Benckiser is recalling Durex Pleasure Pack condoms because five batches failed burst pressure specifications.
Product
Durex Pleasure Pack (60 ct), synthetic polisoprene male condom, SKU 02340-98729-00 02340-98729-00 02340-98729-00 02340-98729-00 02340-98729-00 02340-98729-00
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1167-2019·2019-03-20
Nature's Path Organic Chocolate Choco Chimps Cereal Recalled for Undeclared Gluten
Nature's Path is recalling Organic Chocolate Choco Chimps cereal because it may contain undeclared gluten (wheat and barley).
Product
Nature's Path Organic Chocolate Choco Chimps Organic cereal. Net Wt. 10 oz (284 g), UPC 58449-87024. Nature's Path Foods, Inc., Blaine, WA 98230
Category
Food
Distribution
Distributed nationwide
HighNHTSA·19V218000·2019-03-20
Volkswagen Atlas and Passat Recall for Incorrect Side Air Bags
Volkswagen is recalling 2019 Atlas and 2020 Passat vehicles because incorrect side air bags may have been installed, potentially failing to deploy in a crash.
Product
VOLKSWAGEN — VOLKSWAGEN ATLAS, PASSAT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0993-2019·2019-03-20
Durex Real Feel Condoms Recalled for Burst Pressure Failure
Reckitt Benckiser LLC is recalling Durex Real Feel condoms because five batches failed burst pressure specifications.
Product
Durex Real Feel, synthetic polisoprene male condom, SKU 02340-89456-14 02340-89455-00 02340-89456-14 02340-89456-14 02340-89455-00 02340-95767-00 02340-89456-14 02340-89457-00 02340-89456-14 02340-89456-14 02340-89455-00 02340-89455-00 02340-95767-00 02340-95767-00
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·19V215000·2019-03-20
Thor Motor Coach Recalls 2018-2019 Quantum RW28 Motorhomes for Missing Lights
Thor Motor Coach is recalling 2018-2019 Quantum RW28 motorhomes because they may be missing mid-ship marker lights, which can cause other drivers to underestimate the vehicle's length.
Product
THOR MOTOR COACH — THOR MOTOR COACH QUANTUM
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-1168-2019·2019-03-20
Nature's Path Organic Gorilla Munch Corn Puffs Recalled for Undeclared Gluten
Nature's Path is recalling Organic Gorilla Munch Corn Puffs cereal because it may contain undeclared gluten (wheat and barley). The recall covers 23,969 cases distributed nationwide and internationally.
Product
Nature's Path Organic Gorilla Munch Corn Puffs cereal. Net Wt. 10 oz (284 g), UPC 58449-86002. Nature's Path Foods, Inc., Blaine, WA 98230.
Category
Food
Distribution
Distributed nationwide
HighNHTSA·19V214000·2019-03-20
Fouts Bros Fire Apparatus Recall for Brake Light Wiring Defect
Fouts Bros is recalling 2017-2018 F-3000, F-Rescue, and F-Pumper fire apparatus vehicles because brake lights may illuminate without the brake pedal being pressed.
Product
FOUTS BROS. — FOUTS BROS. F-PUMPER, F-3000, F-RESCUE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-1169-2019·2019-03-20
Nature's Path Organic Cinnamon Jungle Munch Recalled for Undeclared Gluten
Nature's Path is recalling Organic Cinnamon Jungle Munch cereal because it may contain undeclared gluten (wheat and barley).
Product
Nature's Path Organic Cinnamon Jungle Munch cereal. Net Wt. 10 oz (284 g), UPC 58449-87028. Nature's Path Foods, Inc., Blaine, WA 98230.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1011-2019·2019-03-20
US Endoscopy Padlock Clip Recalled for Potential Esophageal Laceration Risk
US Endoscopy Group Inc is recalling Padlock Clip defect closure systems due to a risk of esophageal laceration during patient procedures.
Product
US Endoscopy Padlock Clip defect closure system Ref: C910001 The Padlock Clip is indicated for use in flexible endoscopy and for the compression of tissue in the gastrointestinal tract, for hemostasis or for treating lesions of the wall of the gastrointestinal organs.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·19V222000·2019-03-20
Mercedes-Benz Recalls 2018-2019 Sprinter and Metris Vehicles for Missing Inspection
Daimler Vans USA is recalling 2018-2019 Mercedes-Benz Sprinter and Metris vehicles because they left the plant without final quality inspection of safety-relevant parts.
Product
MERCEDES-BENZ — MERCEDES-BENZ METRIS, SPRINTER 3500, SPRINTER 2500
Category
Vehicle
Distribution
Distributed nationwide