State

Rhode Island product recalls

73,809 recalls have nationwide distribution and so reach Rhode Island. 3,054 additional recalls listed Rhode Island specifically in their distribution scope.

What the numbers show

Total: 3,054
Critical: 221
Severe: 708
Most recent: 2026-11-04

Of the 3,054 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 708 (23%) are Severe.

Which agencies issued them

These figures cover only the 3,054 recalls whose distribution notice names Rhode Island specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44101–44125 of 76863

CriticalFDA (Drugs)·D-0969-2017·2017-07-19
Enhancerol Herbal Supplement Recalled for Undeclared Prescription Drug Ingredients
Organic Herbal Supply is recalling Enhancerol Herbal Dietary Supplement Capsules because FDA analysis found undeclared tadalafil, sildenafil, and Flibanserin.
Product
ENHANCEROL Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Made in Malaysia, Distributed by Organic Herbal Supply, Cheyenne, WY ---- UPC Code 680474229086
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0966-2017·2017-07-19
Tornado Male Enhancement Supplement Recalled for Undeclared Prescription Drugs
Organic Herbal Supply is recalling Tornado Male Enhancement capsules because FDA analysis found undeclared prescription drugs, including tadalafil and sildenafil.
Product
TORNADO Male Enhancement Herbal Dietary Supplement Capsules, Over 4000 mg value, supplied in 2, 4 and 10 count packages, Made in USA Distributed by American Health Supplements, Chicago, Illinois --- UPC Code 680474228959
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0967-2017·2017-07-19
FDA Recalls ZDaily Testosterone Supplement for Undeclared Prescription Drugs
Organic Herbal Supply is recalling ZDaily Testosterone and Libido Booster capsules because FDA analysis found undeclared prescription drugs, including tadalafil, sildenafil, and flibanserin.
Product
ZDaily Daily Testosterone and Llibido Booster Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Distributed by Organic Herbal Supply, Roseville, CA --- UPC Code 680474229062
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0971-2017·2017-07-19
LabidaMAX Herbal Supplement Recalled for Undeclared Prescription Drugs
Organic Herbal Supply is recalling LabidaMAX Herbal Dietary Supplement Capsules because FDA analysis found undeclared prescription drugs.
Product
LabidaMAX Herbal Dietary Supplement Capsules, 500 mg, supplied in 30 count packages, Made in Malaysia, Distributed by Organic Herbal Supply, Cheyenne, WY --- UPC Code 680474228904
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0968-2017·2017-07-19
FDA Recalls BIGnHARD Male Enhancement Capsules for Undeclared Prescription Drugs
Organic Herbal Supply is recalling BIGnHARD Male Enhancement Capsules because FDA testing found undeclared prescription drugs, including tadalafil and sildenafil.
Product
BIGnHARD Male Enhancement Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Made in Malaysia, Distributed by Organic Herbal Supply, Cheyenne, WY ---- UPC Code 680474229086
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0962-2017·2017-07-19
FDA Recalls Cummor Male Enhancement Supplement for Undeclared Prescription Drugs
Organic Herbal Supply is recalling Cummor Natural Male Enhancement capsules because FDA analysis found undeclared prescription drugs, including tadalafil and sildenafil.
Product
Cummor Natural Male Enhancement, Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Made in Malaysia, Distributed by Naturally Hard Supplements, Reno, NV --- UPC code #680474229116
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0963-2017·2017-07-19
ZRECT Male Enhancement Supplement Recalled for Undeclared Prescription Drugs
Organic Herbal Supply is recalling ZRECT Male Enhancement capsules because FDA analysis found undeclared prescription drugs, including tadalafil and sildenafil.
Product
ZRECT Male Enhancement Herbal Dietary Supplement Capsules, 500 mg, supplied in 2, 4 and 10 count packages, Made in Malaysia, Distributed by Organic Herbal Supply, Roseville, CA --- UPC Code 852675999451
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-2539-2017·2017-07-19
Wildway Apple Cinnamon Granola Recalled for Listeria Contamination Risk
Wildway LLC is recalling specific lots of Apple Cinnamon Grain-Free Granola due to potential Listeria monocytogenes contamination.
Product
Wildway Apple Cinnamon Grain-Free Granola 8 oz and 10 oz UPC: 85866005190 and UPC: 864352000015 packaged in plastic bag
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0956-2017·2017-07-19
Advanced Pharma Recalls Potassium Phosphate Injection Due to Sterility Concerns
Advanced Pharma Inc. is recalling specific lots of Potassium Phosphate Injection due to a lack of assurance of sterility. The product was distributed nationwide.
Product
Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL 15 mmol in NS 250mL Bag, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404. NDC15082-922-25
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-2540-2017·2017-07-19
Wildway Banana Nut Granola Recalled for Listeria Contamination Risk
Wildway LLC is recalling 434 cases of Banana Nut Grain-free Granola due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Product
Wildway Banana Nut Grain-free Granola 8 oz. UPC: 858660005176 packaged in a plastic bag
Category
Food
Distribution
Distributed nationwide
SevereCPSC·17190·2017-07-19
Polaris Recalls Sportsman 570 ATVs Due to Fuel Leak and Fire Hazards
Polaris is recalling about 25,600 model year 2014 Sportsman 570 ATVs because fuel can leak into the headlight pod, posing fire hazards.
Product
Sportsman 570 all-terrain vehicles (ATVs)
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-2576-2017·2017-07-19
Wildway LLC Recalls Trader Joe's Grainless Granola Due to Listeria Risk
Wildway LLC is recalling specific lots of Trader Joe's Grainless Granola due to potential contamination with Listeria monocytogenes.
Product
Trader Joe's Grainless Granola 8 oz. (SKU 56307) packaged in a plastic bag
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-2542-2017·2017-07-19
Wildway Vanilla Bean Espresso Granola Recalled for Listeria Risk
Wildway LLC is recalling 442 cases of Vanilla Bean Espresso Grain-free Granola due to potential Listeria monocytogenes contamination.
Product
Wildway Vanilla Bean Espresso Grain-free Granola 8 oz. UPC: 858660005206 packaged in a plastic bag
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0958-2017·2017-07-19
AstraZeneca Recalls BRILINTA Tablets Due to Foreign Zurampic Contamination
AstraZeneca is recalling 40,368 bottles of BRILINTA 90 mg tablets because some bottles contained foreign Zurampic tablets.
Product
BRILINTA — BRILINTA (TICAGRELOR)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2340-2017·2017-07-19
Oscor ATAR Reusable Extension Cables Recalled for Connector Separation Risk
Oscor, Inc. is recalling ATAR Reusable Extension Cables because they may separate from the connector during use, posing a risk to patients.
Product
ATAR Reusable Extension Cable, sold under brand names: ATAR Reusable Series, ATAR 53912 Reusable Series, and XI Reusable Series. Model codes: 53912 - MDTS ATAR REUSABLE, 53912A - MDTS ATAR REUSABLE, ATAR MDTS REUSABLE, ATAR-A DARK BLUE REUSABLE, ATAR-MDT REUSABLE, ATAR-MDT2…
Category
Medical Device
Distribution
39 states
SevereFDA (Drugs)·D-0957-2017·2017-07-19
Baxter Recalls Sodium Chloride Injection Bags Due to Sterility Concerns
Baxter Healthcare is recalling 0.9% Sodium Chloride Injection bags due to customer complaints about leaking bags, which raises concerns about the product's sterility.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0960-2017·2017-07-19
Teva Recalls Paliperidone Extended-Release Tablets Due to Dissolution Failure
Teva Pharmaceuticals is recalling 360 bottles of Paliperidone Extended-Release Tablets because one tablet failed a routine stability test for drug release.
Product
Paliperidone Extended-Release Tablets, 3 mg, 90 count bottles, Rx only, Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314 USA Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054, USA, NDC: 0591-3693-19
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0972-2017·2017-07-19
Baxter Recalls 5% Dextrose Injection Due to Sterility Concerns
Baxter Healthcare is recalling 54,528 bags of 5% Dextrose Injection because the bags may leak, compromising sterility.
Product
DEXTROSE — DEXTROSE (DEXTROSE MONOHYDRATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2733-2017·2017-07-19
Oscor ATAR Disposable Extension Cables Recalled for Connector Separation Risk
Oscor, Inc. is recalling ATAR Disposable Extension Cables because they may separate from the connector during use, posing a risk to patients.
Product
ATAR Disposable Extension Cable, sold under brand names: ATAR Disposable Series, ATAR 53912 Disposable Series, and XI Disposable Series. Model codes: ATAR D-A DARK BLUE DISPOSABLE, ATAR D-V WHITE DISPOSABLE, ATAR D-MDT DISPOSABLE, ATAR D-T DISPOSABLE, ATAR D-R DISPOSABLE…
Category
Medical Device
Distribution
39 states
SevereFDA (Drugs)·D-0959-2017·2017-07-19
Bristol-Myers Squibb Recalls Eliquis 5mg Tablets Due to Labeling Error
Bristol-Myers Squibb is recalling 48,180 bottles of Eliquis 5mg tablets because one bottle was found to contain 2.5mg tablets instead.
Product
EliquisTablets 5mg, 60 count bottle, Rx Only, Marketed by: Bristol-Meyers Squibb Company Princeton, NJ 08543 USA and Pfizer Inc. New York, NY 10017 USA, NDC 0003-0894-21
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·17V450000·2017-07-19
Daimler Trucks Recalls 2017-2018 Freightliner and Western Star Trucks for Fuel Pump Defect
Daimler Trucks is recalling specific 2017-2018 Freightliner and Western Star trucks because a fuel pump drive gear may slip, causing sudden engine stalls and increasing crash risk.
Product
FREIGHTLINER CUSTOM CHASS — FREIGHTLINER CUSTOM CHASS, FREIGHTLINER, WESTERN STAR XCP, 122SD, 6900, XCM
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0953-2017·2017-07-19
Advanced Pharma Recalls Succinylcholine Chloride Injection Due to Sterility Concerns
Advanced Pharma Inc. is recalling QUELICIN (Succinylcholine Chloride) Injection due to a lack of assurance of sterility. The recall affects 2,350 units distributed nationwide.
Product
QUELICIN (Succinylcholine Chloride) Injection, USP 20 mg/mL in a) 5 mL vial (NDC 15082-814-67), b) 7mL vial (NDC 15082-814-79), c) 10mL vial (NDC 15082-814-61), Repackaged by Advanced Pharm, 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0954-2017·2017-07-19
Advanced Pharma Recalls Potassium Phosphate IV Bags Due to Sterility Concerns
Advanced Pharma Inc. is recalling 72 units of Potassium Phosphate IV bags nationwide due to a lack of assurance of sterility.
Product
Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL 20 mmol in NS 250mL Bag, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404. NDC15082-926-25
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0955-2017·2017-07-19
Advanced Pharma Recalls Potassium Phosphate Bags Due to Sterility Concerns
Advanced Pharma Inc. is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride bags because the company cannot assure the product's sterility.
Product
Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL 30 mmol in NS 250mL Bag, Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404. NDC15082-924-25
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2705-2017·2017-07-19
O-Two Adult Ventilation Timer Recalled Due to Flash Rate Malfunction
O-Two Medical Technologies is recalling Adult Ventilation Timers because the flash rate may be twice the labeled rate, potentially affecting ventilation guidance.
Product
O-Two Adult Ventilation Timer, MODEL #(s): 01BM1000-CS, 01BM3201-MOTP-CS, 01BM3201-MOTL-CS, CATALOG #(s): 01BM1000 --- INTENDED USE: The Adult Ventilation Timer is intended to guide the rescuer to provide ventilations at a rate appropriate for adult patients
Category
Medical Device
Distribution
Distributed nationwide