State

Rhode Island product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46476–46500 of 76871

ModerateFDA (Devices)·Z-1086-2017·2017-02-01
Atrium Medical Recalls Oasis Blood Recovery Drains Due to Sterility Issues
Atrium Medical is recalling Oasis Blood Recovery Drains because the outer packaging is not sterile. The recall covers units with expiration dates prior to October 2019.
Product
Atrium Medical Oasis Blood Recovery Drains as follows: 3650-100 Oasis Blood Recovery drain with in-line connector 3652-100 Oasis Double Blood Recovery drain with in-line connectors - 2 patient lines connected by one Y connector Product Usage: To evacuate air and/or fluid…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1087-2017·2017-02-01
Atrium Medical 400 Series Express Drains Recalled for Non-Sterile Packaging
Atrium Medical is recalling 400 Series Express Drains because the outer packaging is not sterile. The recall affects approximately 1.4 million cases distributed worldwide.
Product
Atrium Medical 400 Series Express Drains as follows: 4000-100N Express single collection drain with in-line connector 4000-100P Express PreFilled Chest Drain 4020-100N Express dual chamber drain with in-line connectors ( 2 Patient Tubes) 4050-100N Express Blood Recovery…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0446-2017·2017-02-01
Sun Pharmaceutical Recalls BuPROPion Hydrochloride Tablets for Dissolution Failures
Sun Pharmaceutical Industries is recalling 11,618 bottles of buPROPion Hydrochloride Extended-release Tablets due to failed dissolution specifications and stability issues.
Product
buPROPion Hydrochloride Extended-release Tablets, USP (SR), 200 mg, 60 count bottles, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India NDC…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0442-2017·2017-02-01
Mylan Recalls Temozolomide Capsules Due to Broken Capsules and Loose Powder
Mylan LLC is recalling Temozolomide Capsules, 140 mg, due to customer complaints of broken or crushed capsules resulting in loose powder in the bottles.
Product
Temozolomide Capsules, 140 mg, packaged in a) 5-count bottles (NDC 0378-5263-98), b) 14-count bottles (NDC 0378-5263-14), Rx only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 USA.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1084-2017·2017-02-01
Atrium Medical Oasis Pediatric Drain Recalled for Non-Sterile Packaging
Atrium Medical is recalling Oasis Pediatric Drains because the outer packaging is not sterile. The recall covers 964,463 US cases and 521,975 international cases.
Product
Atrium Medical Oasis Pediatric Drain as follows: 3612-100 Oasis Infant/Pediatric drain with in-line connector, ¿ in. tubing, Sims and Pedi connector in bag on back of drain 3612-400 Oasis Infant/Pediatric drain with no in-line connector, ¿ in. tubing, Sims and Pedi connector…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1088-2017·2017-02-01
Atrium Medical Express Mini 500 Dry Seal Drain Recall
Atrium Medical is recalling Express Mini 500 dry seal drains because the outer packaging is not sterile.
Product
Atrium Medical 16400 Express Mini 500 dry seal drain Product Usage: To evacuate air and/or fluid from the chest cavity or mediastinum. To help re-establish lung expansion and restore breathing dynamics. To facilitate postoperative collection and reinfusion of autologous…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1102-2017·2017-02-01
PerkinElmer AutoDELFIA System Recalled for Potential Plate Loading Failures
PerkinElmer is recalling AutoDELFIA systems with V3.0 software due to potential plate loading failures that could affect clinical assay results.
Product
DELFIA¿ PC with V3.0 Software, Fluorometer, for clinical use Product Number: 1235-8100 Product Usage: The Wallac 1235 AutoDELFIA automatic immunoassay system is designed to automatically perform assays using the DELFIA technology. DELFIA technology is based on the proven…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0448-2017·2017-02-01
Roxane Recalls Azelastine Nasal Spray Due to Defective Delivery System
Roxane Laboratories is recalling 74,108 bottles of Azelastine Hydrochloride Nasal Spray because the delivery system failed droplet size testing.
Product
Azelastine Hydrochloride Nasal Solution (Nasal Spray), 0.1% (137 mcg per spray), packaged in 30 mL bottles, Rx only, Distributed by: West-Ward Pharmaceuticals Corp., Eatontown, NJ 07724, NDC 0054-0293-99
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1101-2017·2017-02-01
PerkinElmer AutoDELFIA System Recalled for Potential Plate Loading Failures
PerkinElmer is recalling AutoDELFIA systems with Version 3.0 software due to potential plate loading failures that could affect clinical assay results.
Product
Program Update Package AutoDELFIA¿ 3.0, Fluorometer, for clinical use Product Number: 1235-8110 Product Usage: The Wallac 1235 AutoDELFIA automatic immunoassay system is designed to automatically perform assays using the DELFIA technology. DELFIA technology is based on the…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0438-2017·2017-02-01
Qualitest Recalls Dexamethasone Elixir Due to Failed Impurity Specifications
Vintage Pharmaceuticals is recalling 2,568 bottles of Dexamethasone Elixir because the product failed impurity and degradation specifications.
Product
DEXAMETHASONE ELIXIR, USP, 0.5 mg/5 mL, 8 fl.oz., Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL, NDC 0603-1147-56
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1075-2017·2017-02-01
Pentax Rigid Laryngostroboscopes Field Correction for Instructions for Use
Pentax of America is revising the Instructions for Use for Rigid Laryngostroboscopes Models 9106 and 9108.
Product
Rigid Laryngostroboscopes The Rigid Laryngostroboscopes, Models 9106 and 9108 are intended to observe glottic action with the use of a stroboscopic light source. The instrument is inserted per-orally when indications consistent with the need for observation are observed.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0439-2017·2017-02-01
Actavis Recalls Albuterol Sulfate Inhalation Solution Due to Impurities
Actavis Inc is recalling specific lots of Albuterol Sulfate Inhalation Solution because the product failed impurity specifications for a known degradant.
Product
Albuterol Sulfate Inhalation Solution, USP, 0.021% (0.63 mg / 3 mL), 3mL Vials, Rx only, Mfd. for Watson Laboratories Inc., Corona, CA 92880 USA, Mfd. by Cipla Ltd. Verna, Goa India, NDC 0591-3467-53
Category
Drug
Distribution
Distributed nationwide
SevereCPSC·17730·2017-01-31
Simpli Home Recalls Chests of Drawers Due to Tip-Over Hazard
Simpli Home is recalling about 240 chests of drawers because they can tip over and injure children if not anchored to the wall.
Product
Chest of drawers
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·17078·2017-01-31
Bar Chairs Recalled Due to Fall Hazard from Detaching Legs
3i Corporation is recalling bar chairs sold at Lowe's because legs can detach from the center post, posing a fall hazard.
Product
Bar chairs
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·17075·2017-01-31
Bolton Furniture Recalls 4-Drawer Dressers Due to Tip-Over Hazards
Bolton Furniture is recalling approximately 1,000 4-drawer dressers because they pose a serious tip-over and entrapment hazard to children if not anchored to the wall.
Product
Two Over Two 4-drawer dressers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·17077·2017-01-31
Brown Jordan Recalls Swivel Patio Chairs Due to Fall Hazard
Brown Jordan Services is recalling La-Z-Boy swivel patio chairs sold at Sears.com because the base can break during normal use, posing a fall hazard.
Product
Swivel Patio Chairs
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·17731·2017-01-31
South Shore Recalls 5-Drawer Chests Due to Tip-Over and Entrapment Hazards
South Shore is recalling 5-drawer chests that pose tip-over and entrapment hazards to children if not anchored to the wall.
Product
5-drawer chests
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·17V064000·2017-01-31
Van Hool Motorcoach Recall for Steering Box Defect in Cold Weather
Van Hool is recalling specific 2010-2017 motorcoaches because the steering wheel may be difficult to turn in low temperatures, increasing crash risk.
Product
VAN HOOL — VAN HOOL TX45, CX45, TD925, T2145
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·17076·2017-01-31
Casual Living Recalls Swivel Patio Chairs Due to Fall Hazard
Casual Living Worldwide is recalling about 2 million swivel patio chairs sold at Home Depot because the base can break, causing falls.
Product
Swivel Patio Chairs
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·17079·2017-01-31
Teufelberger Recalls Static Ropes and Throwlines Due to Fall Hazards
Teufelberger is recalling specific static ropes and throwlines because they are mislabeled as certified to NFPA safety standards, posing fall and injury risks to users.
Product
Static ropes and throwlines
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·17074·2017-01-27
IKEA Recalls MYSINGSÖ Beach Chairs Due to Collapse and Amputation Hazards
IKEA is recalling MYSINGSÖ beach chairs because they can collapse, posing fall and fingertip amputation hazards. Consumers should stop using them and return them for a refund or replacement.
Product
MYSINGSÖ beach chairs
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·17V057000·2017-01-26
GM Recalls 2016-2017 Chevrolet Cruze for Seat-Back Welding Defect
General Motors is recalling 2016-2017 Chevrolet Cruze vehicles because a defective weld in the seat-back recliner mechanism may cause the seat to break in a crash, increasing injury risk.
Product
CHEVROLET — CHEVROLET CRUZE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V059000·2017-01-26
Forest River Recalls 2017-2018 Berkshire and Charleston RVs for Fire Risk
Forest River is recalling 2017-2018 Berkshire and Charleston RVs because a power steering hose may rub a power stud, causing arcing and fluid leaks that increase fire risk.
Product
FOREST RIVER — FOREST RIVER BERKSHIRE, CHARLESTON
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V062000·2017-01-26
BMW Recalls 2016-2017 X1 Vehicles for Passenger Air Bag Defect
BMW is recalling 2016-2017 X1 vehicles because the instrument panel may prevent the front passenger air bag from deploying properly, increasing injury risk in a crash.
Product
BMW — BMW X1 SAV
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V063000·2017-01-26
Hyundai Recalls 2017 Elantra Vehicles Due to Brake Booster Failure Risk
Hyundai is recalling 2017 Elantra vehicles because the brake booster may fail, resulting in a loss of power brake assist and increased stopping distance.
Product
HYUNDAI — HYUNDAI ELANTRA
Category
Vehicle
Distribution
Distributed nationwide