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.

37976–38000 of 76794

ModerateFDA (Drugs)·D-0046-2019·2018-10-24
Premier Value Sterile Saline Nasal Mist Recalled for Quality Concerns
Product Quest Manufacturing LLC is recalling 10,584 cans of Premier Value Sterile Saline Nasal Mist due to manufacturing deviations that could impact product quality.
Product
Premier Value, Sterile Saline Nasal Mist, Saline Nasal Moisturizer (0.9% Sodium Chloride) Solution, 4.25 FL OZ (126 mL) can, Distributed By Chain Drug Consortium, 3301 NW Boca Raton Blvd, Suite 101, Boca Raton, FL 33431, NDC 8 40986 02998 1.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0050-2019·2018-10-24
Product Quest Recalls QC Quality Choice Saline Nasal Spray for CGMP Deviations
Product Quest Manufacturing LLC is recalling QC Quality Choice Saline Nasal Spray due to manufacturing deviations that could impact product quality.
Product
QC Quality Choice, Saline Nasal Relief, Moisturizing Nasal Spray, Sodium Chloride 0.65%, packaged as a) 1.5 FL OZ (45 mL) bottle UPC 6 35515 98845 3; b) 3 FL OZ (89 mL) bottle UPC 6 35515 95042 9, Distributed by C.D.M.A., Inc., 43157 W. Nine Mile, Novi, MI 48376-0995.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0079-2019·2018-10-24
Finafta Baby Oral Gel Recalled for Manufacturing Quality Deviations
Product Quest Manufacturing LLC is recalling Finafta Baby Oral Gel because it was manufactured under conditions that could impact product quality.
Product
Finafta Baby, Oral Gel (benzocaine 7.5%), 7.1 Grams (0.25 Oz.) tube, Distributed By: Efficient Laboratories, Inc., Miami, FL 33166.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0037-2019·2018-10-24
Product Quest Recalls DG Health Nasal Pump Mist for CGMP Deviations
Product Quest Manufacturing LLC is recalling 786,720 bottles of DG Health No Drip Nasal Pump Mist due to manufacturing deviations that could impact product quality.
Product
DG health, No Drip, Nasal Pump Mist (oxymetazoline hydrochloride), 0.05%, 1 FL OZ (30 mL) bottle, Distributed by: Dolgencorp, LLC, 100 Mission Ridge, Goodlettsville, TN 37072, UPC 7 27510 00373 3 .
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0048-2019·2018-10-24
Premier Value Saline Nasal Spray Recalled for Quality Concerns
Product Quest Manufacturing LLC is recalling Premier Value Saline Nasal Spray due to manufacturing deviations that could impact product quality.
Product
Premier Value, Saline Nasal Spray, Sodium Chloride 0.65%, packaged as a) 3 FL OZ (88 mL) bottle NDC 68016-388-00 UPC 8 40986 01483 3; b) 1.5 FL OZ (44 mL) bottle NDC 68016-466-00 UPC 8 40986 01482 6, Distributed By Chain Drug Consortium, 3301 NW Boca Raton Blvd, Suite 101, Boca…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0058-2019·2018-10-24
FDA Recalls Best Choice Nasal Spray Due to Manufacturing Quality Issues
Product Quest Manufacturing LLC is recalling 3,600 bottles of Best Choice Nasal Spray because they were manufactured under conditions that could impact product quality.
Product
Best Choice, 12 Hour No-Drip Nasal Spray (Oxymetazoline Hydrochloride 0.05%) Nasal Decongestant, 1 FL OZ (30 mL) bottle, Proudly Distributed By: Valu Merchandisers, Co., 5000 Kansas Ave, Kansas City, KS 66106, UPC 0 70038 59895 4.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0035-2019·2018-10-24
CVS Health Saline Nasal Spray Recalled for Manufacturing Deviations
Product Quest Manufacturing LLC is recalling 552 bottles of CVS Health Saline Nasal Spray due to CGMP deviations that could impact product quality.
Product
CVS Health, Saline Nasal Spray, 1.5 FL OZ bottle, Distributed by CVS Pharmacy, Inc. One CVS Drive Woonsocket, RI 02895, Product #277790.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0141-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Issues
Zimmer Biomet is recalling 27 Affixus Hip Fracture Nails because sterile packaging was found open during surgery.
Product
Affixus Hip Fracture Nail Right 125 13 mm x 300 mm, Item Number 814313300 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0061-2019·2018-10-24
Walgreens NO DRIP Anefrin Nasal Spray recall due to CGMP deviations
This FDA drug recall affects Walgreens NO DRIP Anefrin nasal spray due to current good manufacturing practice deviations that could impact product quality.
Product
Walgreens, NO DRIP Anefrin Nasal Spray (Oxymetazoline HCl 0.05%), Nasal Decongestant, Extra Moisturizing, 12 Hour, 0.5 FL OZ (15 mL) bottle, Distributed By: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-7004-01, UPC 3 11917 18534 7.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0047-2019·2018-10-24
FDA Recalls Premier Value Nasal Decongestant Spray Due to Quality Concerns
Product Quest Manufacturing LLC is recalling Premier Value Nasal Decongestant Nasal Spray because it was manufactured under conditions that could impact product quality.
Product
Premier Value, Nasal Decongestant, Nasal Spray (oxymetazoline HCl 0.05%), Regular Strength, 1 FL OZ (30 mL) bottle, Distributed By Chain Drug Consortium, 3301 NW Boca Raton Blvd, Suite 101, Boca Raton, FL 33431, NDC 68016-316-03, UPC 8 40986 01516 8.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0144-2019·2018-10-24
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Issues
Zimmer Biomet is recalling 25 Affixus Hip Fracture Nails because sterile packaging was found open during surgery. The recall covers units distributed in the US and abroad.
Product
Affixus Hip Fracture Nail Right 125 13 mm x 440 mm, Item Number 814313440 Product Usage: Intended for the fixation of fractures
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0069-2019·2018-10-24
Well at Walgreens Scar Cream Recalled for Low Active Ingredient Levels
Product Quest Manufacturing LLC is recalling 6,516 tubes of Well at Walgreens Scar Cream with SPF 30 because the octocrylene and avobenzone levels were found to be lower than required.
Product
Well at Walgreens, Scar Cream with SPF 30, (Avobenzone 3%, Octocrylene 10%, Oxybenzone 6%), 0.7 OZ (19.8 g) tube, Distributed By: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, UPC 3 11917 18281 0.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0249-2019·2018-10-24
Amerigen Recalls Temozolomide Capsules Due to Dissolution Failures
Amerigen Pharmaceuticals is recalling Temozolomide capsules because stability testing revealed out-of-specification dissolution results.
Product
Temozolomide capsules, 20 mg, packaged in a) 5-count bottle(NCD 43975-253-05), b) 14-count bottle (NDC 43975-253-14), Rx only, Mfd. by: Stason Pharmaceuticals, Inc., Irvine, CA 92618, Dist. By: Amerigen Pharmaceuticals, Lyndhurst, NJ 07071.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0070-2019·2018-10-24
Cicatricure Scar Cream Recalled for Low Active Ingredient Levels
Product Quest Manufacturing LLC is recalling Cicatricure Scar Cream + Sunscreen SPF 30 because the octocrylene and avobenzone levels were found to be lower than required.
Product
Cicatricure, Scar Cream + Sunscreen SPF 30 (avobenzone 3%, octocrylene 10%, oxybenzone 6%), 0.7 oz. (19.8 g) tube, Distributed by: Genomma Lab USA Inc., Houston, TX 77027, UPC 6 50067 00018 7.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·18V750000·2018-10-23
Proterra Recalls 2016-2017 Catalyst Buses Due to Brake Caliper Defect
Proterra is recalling 2016-2017 Catalyst transit buses because a defect in the brake calipers may cause the guide pin support bolt to break, potentially leading to loss of braking ability or tire pressure.
Product
PROTERRA — PROTERRA CATALYST
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·19018·2018-10-23
Zeagle Sport Buoyancy Control Devices Recalled Due to Drowning Hazard
Huish Outdoors is recalling Zeagle Sport buoyancy control devices because inflator buttons can break, causing rapid air loss or auto-inflation that poses a drowning risk to scuba divers.
Product
Zeagle Sport buoyancy control devices (BCDs)
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·18V748000·2018-10-22
E-One Recalls 2016-2018 Typhoon and Cyclone II Aerial Devices
E-One is recalling 2016-2018 Typhoon and Cyclone II aerial devices because a torque rod tower may crack, potentially affecting vehicle handling and increasing crash risk.
Product
E-ONE — E-ONE TYPHOON, CYCLONE II
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V747000·2018-10-22
E-One Recalls 2012-2015 Emergency Vehicles Due to Fire Risk
E-One is recalling 2012-2015 Typhoon, Cyclone II, and Cyclone III emergency vehicles because a melting relay in the HVAC system can increase the risk of a fire.
Product
E-ONE — E-ONE CYCLONE II, TYPHOON, CYCLONE III
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V735000·2018-10-22
Ford Recalls 2012-2018 Focus Models Due to Fuel System Defect
Ford is recalling 2012-2018 Focus vehicles with 2.0L engines because a malfunctioning valve may cause the engine to stall while driving, increasing crash risk.
Product
FORD — FORD FOCUS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18V749000·2018-10-22
E-One Recalls 2017 Classic Fire Vehicles Due to Pump Wiring Defect
E-One is recalling 2017 Classic Fire emergency vehicles equipped with specific Kubota pumps that may be improperly wired, preventing warning lamps from illuminating.
Product
E-ONE — E-ONE CLASSIC FIRE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18V746000·2018-10-22
KME Commercial Skid Recall for Improperly Wired Pump Warning Lamps
Kovatch Mobile Equipment is recalling 2015 and 2017 KME Commercial Skids because improperly wired pumps may fail to display oil pressure and temperature warnings.
Product
KME — KME COMMERCIAL SKID
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18V745000·2018-10-22
Altec Recalls 2014-2018 Digger Derrick Vehicles for Software Defect
Altec is recalling 2014-2018 Digger Derrick vehicles because the Zone Rating System may fail to alert operators to excessive loads, increasing injury risk.
Product
ALTEC — ALTEC DIGGER DERRICK
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·103-2018·2018-10-21
Bakkavor Recalls Meat and Poultry Products Due to Possible Salmonella and Listeria
Bakkavor Foods USA is recalling approximately 795,261 pounds of ready-to-eat meat and poultry products containing onions that may be contaminated with Salmonella and Listeria monocytogenes.
Product
Bakkavor Foods USA, Inc. Recalls Meat and Poultry Products due to Possible Salmonella and Listeria monocytogenes Contamination In Onions
Category
Food
Distribution
Distributed nationwide
CriticalUSDA FSIS·098-2018·2018-10-19
Ruiz Food Products Recalls Taquitos Due to Salmonella and Listeria Concerns
Ruiz Food Products is recalling approximately 2.5 million pounds of ready-to-eat beef and poultry taquitos due to possible Salmonella and Listeria contamination in onion ingredients.
Product
Ruiz Food Products, Inc. — Ruiz Food Products, Inc. Recalls Beef and Poultry Products due to Possible Salmonella and Listeria monocytogenes Contamination in Onion Ingredient
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·18V740000·2018-10-19
Chrysler Recalls Pacifica Plug-in Hybrids for Engine Restart and Fire Risk
Chrysler is recalling 2017-2018 Pacifica Plug-in Hybrids because the engine may fail to restart, causing unburned fuel to enter the exhaust and increasing crash or fire risks.
Product
CHRYSLER — CHRYSLER PACIFICA PLUG-IN HYBRID
Category
Vehicle
Distribution
Distributed nationwide