State

Rhode Island product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

55051–55075 of 76881

HighFDA (Devices)·Z-2076-2015·2015-07-22
Sorin Stockert Heater-Cooler 3T Recalled for Potential Organism Colonization
Sorin Group USA, Inc. is recalling 2,837 Sorin Stockert Heater-Cooler 3T units due to potential colonization of organisms, including Mycobacteria, if proper disinfection and maintenance are not performed.
Product
Sorin Stockert Heater-Cooler 3T, 230 V Temperature control for extracorporeal perfusion of durations up to 6 hours.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2062-2015·2015-07-22
Stryker Woundcare Replacement Kits Recalled for Potential Sterility Breach
Stryker is recalling Woundcare Replacement Kits used for wound debridement due to a potential sterility breach in the packaging.
Product
0210-312-000-Woundcare Replacement kit with soft tip; 0210-318-000; Woundcare Replacement with fan tip; 0210-318-100- Woundcare Replacement Kit; 0210-318-200-Woundcare Replacement with retract coax tip. Accessory to Stryker InterPulse Irrigation System, used for wound…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2093-2015·2015-07-22
Northern Digital recalls disposable reflective marker spheres for surgical tracking
Northern Digital Inc. is recalling 32,400 disposable reflective marker spheres used in Brainlab IGS systems due to inadequate adhesive curing that may cause the spheres to separate.
Product
NDI Disposable Reflective Marker Spheres for Brainlab IGS (Image Guided Surgery) system. Product Usage: Disposable reflective marker spheres are attached to reference arrays and instruments, thus enabling the infrared tracking systems to detect the position of the patient…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15V460000·2015-07-22
Chrysler Recalls 2013-2015 Ram Trucks for Air Bag Deployment Risk
Chrysler is recalling 2013-2015 Ram 1500, 2500, and 3500 trucks because side air bags and seat belts may deploy unexpectedly, increasing crash risk.
Product
RAM — RAM 3500, 2500, 1500
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2073-2015·2015-07-22
Etac Supporter toilet armrest recalled due to loose fasteners
Etac Supply Center Ab is recalling 25 units of Supporter toilet armrests because fasteners may come loose, causing the product to become unsteady.
Product
Etac Supporter toilet armrest Etac Supporter toilet armrests are foldable and have comfortable rounded grips for the hands. Supporter is simple to mount without the need for any tools. It fits both floor and wall mounted toilets. If space around the toilet is limited either…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2078-2015·2015-07-22
Sorin Stockert Heater-Cooler 3T Recalled for Potential Organism Colonization
Sorin Group USA is recalling 283 Sorin Stockert Heater-Cooler 3T units due to potential colonization of organisms, including Mycobacteria, if proper disinfection is not performed.
Product
Sorin Stockert Heater-Cooler 3T, 208 V / 60 Hz Temperature control for extracorporeal perfusion of durations up to 6 hours.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2095-2015·2015-07-22
Alere i Influenza A & B Kit Recalled for False Negative Risk
Alere is recalling 257 kits of the Alere i Influenza A & B test due to microbial growth that may cause false negative results.
Product
Alere i flu, Alere i, Alere Influenza A & B; Part Number (PN) 425-024 The Alere" i Influenza A & B assay, performed on the Alere" i Instrument, is a rapid molecular in vitro diagnostic test utilizing an isothermal nucleic acid amplification technology for the qualitative…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2084-2015·2015-07-22
NDI Disposable Reflective Marker Spheres Recalled for Adhesive Defect
Northern Digital Inc. is recalling NDI Disposable Reflective Marker Spheres because inadequate adhesive curing may cause the spheres to separate.
Product
NDI Disposable Reflective Marker Spheres for Brainlab IGS (Image Guided Surgical) system. Product Usage: Disposable reflective marker spheres are attached to reference arrays and instruments, thus enabling the infrared tracking systems to detect the position of the patient…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2092-2015·2015-07-22
Synthes Recalls RIA Drive Shafts and Reamer Heads Due to Breakage Risk
Synthes, Inc. is recalling Reamer / Irrigator / Aspirator (RIA) components because they may break if incorrectly assembled or used improperly.
Product
Reamer / Irrigator / Aspirator (RIA): RIA Drive Shafts, RIA Tube Assemblies, sterile, RIA Reamer Head, sterile (12.0mm-19.0mm); intended to clear the medullary canal of bone marrow and debris and to effectively size the medullary canal for the acceptance of an intramedullary…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15V458000·2015-07-22
Kenworth Trucks Recalled for Hazard Light Override Defect
PACCAR is recalling 2011-2016 Kenworth trucks because daytime running lamps may override hazard warning lights, increasing crash risk.
Product
KENWORTH — KENWORTH T440, T470, T880, T680
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2080-2015·2015-07-22
Sorin Heater-Cooler Devices Recalled for Potential Microbial Colonization
Sorin Group USA is recalling Stockert Heater-Cooler 3T devices due to the potential for microbial colonization, including Mycobacteria, if proper disinfection and maintenance are not performed.
Product
Sorin Stockert Heater-Cooler 3T, 120 V / 60 Hz Temperature control for extracorporeal perfusion of durations up to 6 hours.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2065-2015·2015-07-22
Biomet Oxford Femoral Drill Guide Recalled for Undersized Diameter
Biomet is recalling 18 Oxford Femoral Drill Guide Lateral IM Adapters because an undersized diameter may interfere with a specific IM Link component.
Product
Oxford Femoral Drill Guide Lateral IM Adapter Product Usage: Drill guide. The Oxford Fixed Bearing Knee is a Partial knee replacement system consisting of a femoral component and a fixed bearing tibial component for use in the lateral compartment of the knee. Partial…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2088-2015·2015-07-22
Eizo RadiForce RX650 LCD Monitor Recalled for Display Abnormalities
Eizo is recalling RadiForce RX650 LCD monitors that may display abnormally when connected to specific graphics boards using DisplayPort.
Product
RadiForce RX650, 6MP Color LCD Monitor, Part Code No. 0FTD1957A5, 0FTD195B5, UPC 690592037203. This product is intended to be used in displaying and viewing digital images for review and analysis by trained medical practitioners. It does not support the display of mammography…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1237-2015·2015-07-22
Kremers Urban Recalls Nitroglycerin Transdermal Patches Due to Impurity Failure
Kremers Urban Pharmaceuticals is recalling 16,504 boxes of Nitroglycerin Transdermal Systems because two lots failed impurity specifications during stability testing.
Product
Nitroglycerin Transdermal System 0.4 mg/hr (18 cm2), For Transdermal Use Only, 30 Systems (patches) per box, Rx Only, Manufactured for: Kremers Urban Pharmaceuticals Inc., Princeton, NJ, 08540, USA, By LTS Lohmann Therapie Systeme AG, Anderach, Federal Republic of Germany, NDC…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2070-2015·2015-07-22
Exactech Recalls Four Ambassador Cervical Plate Systems
Exactech, Inc. is recalling four Ambassador Cervical Plate Systems that were shipped to a single consignee in Florida before final inspection was completed.
Product
Exactech Ambassador Cervical Plate System The Exactech Ambassador Cervical Place System is intended for anterior cervical fixation (C2-T1) for the following: degenerative disc disease (DDD) (defined as neck pain of discogenic origin with degeration of the disc confirmed by…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2067-2015·2015-07-22
Nidek Green Laser Photocoagulator Accessories Recalled for Missing Labels
Nidek Inc is recalling 22 units of GYC-1000 laser accessories because they are missing required Laser Aperture labels.
Product
Dual Delivery 4DD-1 of GYC-1000 Green Laser Photocoagulator system GYC4DD-1: The Nidek Green Laser Photocoagulator Model GYC- 1000 is indicated for use in ophthalmic surgical procedures, including retinal and macular photocoagulation, iridotomy and trabeculoplasty.
Category
Medical Device
Distribution
14 states
ModerateFDA (Drugs)·D-1242-2015·2015-07-22
Hospira Recalls Ketorolac Tromethamine Injections Due to Crystallization
Hospira Inc. is recalling specific lots of Ketorolac Tromethamine Injection due to the presence of crystals identified as the calcium salt of Ketorolac.
Product
KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2068-2015·2015-07-22
Nidek GYC-1000 Laser Accessories Recalled for Missing Labels
Nidek Inc is recalling GYC-1000 laser accessories because they are missing Laser Aperture labels. The affected units were distributed to 13 US states.
Product
Endophotocoagulation Delivery 4EP-1 of GYC-1000 Green Laser Photocoagulator System; GYC4EP-01 0W02 and GYC4EP-1 0Z20; The Nidek Green Laser Photocoagulator Model GYC- 1000 is indicated for use in ophthalmic surgical procedures, including retinal and macular photocoagulation…
Category
Medical Device
Distribution
14 states
ModerateFDA (Devices)·Z-2071-2015·2015-07-22
Exactech Single Barrel Drill Guides Recalled for Incomplete Final Inspection
Exactech, Inc. is recalling two Single Barrel Drill Guides shipped to a single consignee in Florida before final inspection was completed.
Product
Exactech Single Barrel Drill Guides The Single Barrel Drill Guide is a nonpowered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2075-2015·2015-07-22
Musculoskeletal Transplant Foundation Recalls Allofix Insertion Kits Due to Drill Size Labeling Error
Musculoskeletal Transplant Foundation is recalling 117 Allofix Insertion Kits because they are labeled as 2.0mm but may contain 2.4mm drills.
Product
Allofix Insertion Kit, 2.0 mm, Single Drill, Product Usage: MTF Surgical Instruments are designed for the specific needs of the orthopedic surgeon and are intended to be used in conjunction with the associated allograft. This kit is for single use only.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1241-2015·2015-07-22
Hospira Recalls Ketorolac Tromethamine Injections Due to Crystallization
Hospira Inc. is recalling Ketorolac Tromethamine Injections because crystallization was identified as the calcium salt of Ketorolac.
Product
KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2074-2015·2015-07-22
Nobel Biocare Recalls Zirconia Abutment Retrieval Instruments Due to Dimensional Error
Nobel Biocare is recalling 149 units of Zirconia Abutment Retrieval Instruments and Kits because a dimensional error prevents the instruments from removing metal adapters as intended.
Product
Abutment Retrieval Instrument Zirconia CC RP/WP, Article No. 37882 and Abutment Retrieval Kit, Article No. 37508 (Article No. 37882 was assembled in this kit). Used to remove a zirconia abutment if the abutment is stuck in the implant connection due to a tight seat. Endosseous…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2087-2015·2015-07-22
Eizo RadiForce GX540 Monitors Recalled for Display Abnormalities
Eizo is recalling 19 RadiForce GX540 monitors that may display abnormally when connected to specific graphics boards with DisplayPort.
Product
RadiForce GX540, 5MP Monochrome LCD Monitor, Part Code No. 0FTD1826A5, 0FTD1826B5, 0FTD1826C5, UPC 690592034752. This product is intended to be used in displaying and viewing digital images including those of digital mammography for review and analysis by trained medical…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2091-2015·2015-07-22
Synthes Recalls Helical Blade Inserter for TFNA Due to Sizing Defect
Synthes (USA) Products LLC is recalling 32 units of the Helical Blade Inserter for TFNA because an oversized pin prevents the tool from passing through the guide sleeve.
Product
Helical Blade Inserter for Trochanteric Fixation Nail-ADVANCED (TFNA); intended to secure the head element to the head element inserter to prevent disengagement during head element insertion. Manual orthopedic surgical instrument.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1235-2015·2015-07-22
Desmopressin Acetate Tablets Recalled for Incorrect Imprint
American Health Packaging is recalling Desmopressin Acetate Tablets because some are incorrectly imprinted with an X on one side.
Product
Desmopressin Acetate Tablets, 0.1 mg Tablets, Rx Only, Packed in 30 Tablet (3 x 10) Cartons. Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217. NDC: 68084-606-21.
Category
Drug
Distribution
Distributed nationwide