State

Rhode Island product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

55876–55900 of 76887

HighFDA (Devices)·Z-1639-2015·2015-05-27
Richard Allan Scientific Recalls Mucolytic Agent Due to Fungal Contamination
Richard Allan Scientific is recalling Mucolytic Agent and Mucolexx after a customer complaint reported fungal contamination in two lots of Mucolexx.
Product
Mucolytic Agent 1 pint/473 ml; 1 gallon/3.8 l Product Usage: A mucoliquefying preservative designed for use in the preparation of mucoid cytology specimens. Mucolexx & Mucolytic Agent liquefies mucus and allows for optimal cytologic diagnostic results.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1628-2015·2015-05-27
Baxter ABACUS Software Recalled for Potential TPN Formula Loading Errors
Baxter is recalling ABACUS SE and ME software because it may load incorrect total parenteral nutrition formulas when duplicate order numbers are used.
Product
ABACUS SE (Single-Workstation Edition) and ABACUS ME (Multi-Workstation Edition) Product Usage: The ABACUS Software is a Windows-based order entry software application for comprehensive total parenteral nutrition (TPN) calculations and label printing.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1642-2015·2015-05-27
DeRoyal Specimen Retrieval Bags Recalled for Tearing During Use
DeRoyal Industries is recalling 5,359 Medium Specimen Retrieval Bags because they may tear or come apart during laparoscopic procedures.
Product
DeRoyal(R) Medium Specimen Retrieval Bag, REF 5500-000-003, Rx Only Product Usage: The device is a single-use specimen retrieval bag indicated for use in laparoscopic procedures to capture and remove organs or tissue from the body cavity.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1622-2015·2015-05-27
Roche Homocysteine Test System Recalled for Inaccurate Low Results
Roche Diagnostics is recalling Homocysteine Reagent lots due to complaints of under-recovery and falsely low patient results, which could delay diagnosis of peripheral vascular disease.
Product
Homocysteine test system - Homocysteine Reagent. 05385415190; Homocysteine 100 Tests, cobas c, COBAS INTEGRA Homocysteine Enzymatic Assay is an in vitro test for the quantitative determination of total L-homocysteine in human serum and plasma on Roche/Hitachi cobas c…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15V315000·2015-05-27
Toyota Recalls 2015 Tundra for Incorrect Tire Pressure Placard
Southeast Toyota Distributors is recalling 144 model year 2015 Toyota Tundra vehicles because the tire placard lists incorrect inflation pressure, which could lead to underinflation and tire failure.
Product
TOYOTA — TOYOTA TUNDRA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1640-2015·2015-05-27
Richard-Allan Scientific Recalls Mucolexx Mucolytic Agent Due to Fungal Contamination
Richard-Allan Scientific is recalling Mucolexx mucolytic agent and Mucolexx products after a customer reported fungal contamination in two lots.
Product
Lerner Laboratories Mucolexx, 1 pint / 473 ml & 1 gallon/3.8 L; Shandon Mucolexx 500ml/0.13gal, 4L/1.06 gal, 120mL Product Usage: A mucoliquefying preservative designed for use in the preparation of mucoid cytology specimens. Mucolexx & Mucolytic Agent liquefies mucus…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1634-2015·2015-05-27
Stryker Scorpio femoral component recall due to blister seal strength
Stryker Howmedica Osteonics is recalling 1,147 Scorpio femoral components because the inner blister peel strength may be below validated requirements, potentially affecting sterile barrier shelf life.
Product
Stryker Orthopaedics Scorpio femoral component. Howmedica Osteonics Corp., A subsidiary of Stryker Corporation Made in USA Sterile. For use in total reconstructive replacement of the knee joint.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1635-2015·2015-05-27
Stryker Triathlon Femoral Component Recalled for Sterile Barrier Seal Issues
Stryker Howmedica Osteonics is recalling 1,147 Triathlon femoral components because the inner blister seal strength may be below validated requirements, potentially affecting sterile shelf life.
Product
Stryker Orthopaedics Triathlon femoral component. Howmedica Osteonics Corp., A subsidiary of Stryker Corporation Made in USA Sterile. For use in total reconstructive replacement of the knee joint
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1633-2015·2015-05-27
Stryker Howmedica Hip Prosthesis Components Recalled for Seal Defects
Stryker Howmedica is recalling 1,147 RESTORATION Acetabular Augment System components because the inner blister seal strength may be below validated requirements, potentially affecting sterile shelf life.
Product
Stryker Howmedica Osteonics RESTORATION Acetabular Augment System; Howmedica Osteonics Corp., A subsidiary of Stryker Corporation Made in USA Sterile. Hip prosthesis component. The RESTORATION Acetabular Wedge Augments provide multiple options to address the wide range of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1626-2015·2015-05-27
Wright Medical Recalls Phalinx Hammertoe Handles Due to Incorrect Laser Etching
Wright Medical Technology is recalling 124 units of Phalinx Hammertoe Handles because the term DORSAL was laser etched on the incorrect side.
Product
PHALINX (TM) HAMMERTOE HANDLE, SIZE: MEDIUM, STYLE: ANGLED, REF 45304013, CONTENTS 1 EACH, RX ONLY
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1636-2015·2015-05-27
MelaFind Device Recalled for Unapproved User Interface Data Display
MELA Sciences is recalling 65 MelaFind devices because the probability and histogram data displayed in the user interface lacks FDA approval.
Product
MelaFind Device, Model MF 100 US, optical diagnostic device for melanoma detection.
Category
Medical Device
Distribution
21 states
ModerateFDA (Devices)·Z-1627-2015·2015-05-27
Wright Medical Recalls PHALINX Hammertoe Handles Due to Incorrect Laser Etching
Wright Medical Technology is recalling 126 units of PHALINX Hammertoe Handles because the term 'DORSAL' was laser etched on the incorrect side.
Product
PHALINX (TM) HAMMERTOE HANDLE, SIZE: LARGE, STYLE: ANGLED, REF 45304014, CONTENTS 1 EACH, RX ONLY
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1554-2015·2015-05-27
Philips DigitalDiagnost X-Ray System Recalled for Missing Exposure Beep Signal
Philips Medical Systems is recalling 54 DigitalDiagnost X-Ray systems because they fail to emit a beep signal after exposure if powered on for over 12 hours.
Product
Philips Healthcare DigitalDiagnost System X-Ray
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1625-2015·2015-05-27
Wright Medical Recalls Phalinx Hammertoe Handle Due to Incorrect Etching
Wright Medical Technology is recalling 121 units of Phalinx Hammertoe Handles because the word 'DORSAL' was laser-etched on the incorrect side.
Product
PHALINX (TM) HAMMERTOE HANDLE, SIZE: SMALL, STYLE: ANGLED, REF 45304012, CONTENTS 1 EACH, RX ONLY
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1555-2015·2015-05-27
Philips DuraDiagnost X-Ray System Recalled for Missing Exposure Beep
Philips Medical Systems is recalling DuraDiagnost X-ray systems because they may fail to emit a termination beep after 12 hours of operation, violating safety regulations.
Product
Philips Healthcare DuraDiagnost X- Ray
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1624-2015·2015-05-27
Wright Medical Recalls Phalinx Hammertoe Handles Due to Incorrect Laser Etching
Wright Medical Technology is recalling 126 units of Phalinx Hammertoe Handles because the term DORSAL was laser etched on the incorrect side.
Product
PHALINX (TM) HAMMERTOE HANDLE, SIZE: X-SMALL, STYLE: ANGLED, REF 45304011, CONTENTS 1 EACH, RX ONLY
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1083-2015·2015-05-27
Mylan Recalls Fexofenadine Hydrochloride Tablets Due to Impurity Levels
Mylan Institutional, Inc. is recalling 1,363 cartons of Fexofenadine Hydrochloride 60 mg tablets because routine stability testing showed slightly above specification results for a related compound.
Product
Fexofenadine Hydrochloride Tablets, USP 60 mg, Allergy, Non-Drowsy, Antihistamine, 100 tablets (10 X 10) per UD Cartons, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV 26505, USA, NDC 51079-547-20
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1630-2015·2015-05-27
CooperSurgical Recalls Carter-Thomason II Port Closure System Due to Printing Defect
CooperSurgical is recalling 430 units of the Carter-Thomason II Port Closure System because pad printing on the suture guide may flake off.
Product
Carter-Thomason II Port Closure System; Model Number(s) CTI-1015P, for use in endoscopic and laparoscopic surgery.
Category
Medical Device
Distribution
Distributed nationwide
CriticalNHTSA·15V313000·2015-05-26
Chrysler Recalls Vehicles Due to Driver Air Bag Inflator Rupture Risk
Chrysler is recalling specific 2004-2011 Dodge, Chrysler, and Mitsubishi vehicles because the driver's air bag inflator may rupture during deployment, potentially causing serious injury or death.
Product
MITSUBISHI — MITSUBISHI, DODGE, CHRYSLER RAIDER, CHARGER, DURANGO, ASPEN
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V310000·2015-05-26
PACCAR Recalls Kenworth and Peterbilt Trucks for Driveshaft Weld Failure
PACCAR is recalling specific Kenworth and Peterbilt trucks because a driveshaft weld may fail due to corrosion, potentially causing loss of power to the rear wheels.
Product
KENWORTH — KENWORTH, PETERBILT T680, 587, T660, T800
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V312000·2015-05-26
Dodge Ram Trucks Recalled for Air Bag Inflator Rupture Risk
Chrysler is recalling 2003 Dodge Ram trucks because the passenger air bag inflator may rupture during deployment, potentially causing serious injury or death.
Product
DODGE — DODGE RAM 3500, RAM 2500, RAM 1500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V309000·2015-05-26
PACCAR Recalls Kenworth and Peterbilt Trucks Due to Fire Risk
PACCAR is recalling specific Kenworth and Peterbilt trucks because a vent tube may detach, allowing engine oil to contact hot surfaces and cause a fire.
Product
PETERBILT — PETERBILT, KENWORTH 365, 384, 348, 382
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·15V308000·2015-05-26
Open Range Recalls 2015 Fifth Wheel Trailers Due to Step Rivet Failure
Open Range R.V. Company is recalling 122 model year 2015 Roamer, Mesa Ridge, and 3X fifth wheel trailers because a rivet on the entry steps may shear, causing the steps to fail.
Product
OPEN RANGE — OPEN RANGE 3X, ROAMER, MESA RIDGE
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·15149·2015-05-26
BRP Recalls Youth Can-Am ATVs for Federal Standard Violations
Bombardier Recreational Products is recalling about 12,500 youth Can-Am ATVs because they fail to meet federal speed and parking brake requirements, posing a crash hazard.
Product
All-terrain vehicles (ATVs)
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·15148·2015-05-26
Gerber Recalls Cohort Folding Knives Due to Laceration Hazard
Gerber is recalling Cohort folding knives because the locking mechanism can fail, posing a laceration hazard. Six injuries have been reported.
Product
Cohort Folding Knife
Category
Consumer Product
Distribution
Distributed nationwide