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.

37376–37400 of 76794

SevereFDA (Devices)·Z-0448-2019·2018-11-21
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect
Zimmer Biomet is recalling 2,163 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Product
Affixus Hip Fracture Nail Left 125 Deg 11x300mm, Item Number 814411300 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullary hip screw to stabilize fractures of the proximal femur.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0413-2019·2018-11-21
GE Healthcare Recalls Aisys Anesthesia System Touchscreen Display Kits
GE Healthcare is recalling 4,207 Aisys anesthesia system touchscreen display kits because they fail to transition to backup ventilation if a patient stops breathing.
Product
Touchscreen display kit. Sold under the following product names: TOUCHSCREEN DISPLAY KIT 11.X ENGLISH FOR USA, TOUCHSCREEN DISPLAY KIT 11.X ENGLISH, TOUCHSCREEN DISPLAY KIT 11.X GERMAN, TOUCHSCREEN DISPLAY KIT 11.X DUTCH, TOUCHSCREEN DISPLAY KIT 11.X FRENCH, TOUCHSCREEN…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0371-2019·2018-11-21
GE Healthcare Millennium MC Medical Device Recall for Detachment Risk
GE Healthcare is recalling 18 Millennium MC units because a detector can detach and fall.
Product
GE Healthcare Millennium MC
Category
Medical Device
Distribution
50 states
SevereNHTSA·18V826000·2018-11-21
Navistar Recalls 2018-2019 International Trucks for Clutch Assembly Defect
Navistar is recalling certain 2018-2019 International trucks because a clutch component may fail, causing unintended vehicle movement and increasing crash risk.
Product
INTERNATIONAL — INTERNATIONAL RH, MV, LONESTAR, HV
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0259-2019·2018-11-21
Sandoz Recalls Isosorbide Dinitrate Tablets Due to Cross Contamination
Sandoz Inc. is recalling Isosorbide Dinitrate Tablets 5 mg due to cross-contamination with other products. The recall affects 7,817 bottles distributed nationwide.
Product
Isosorbide Dinitrate Tablets, USP 5 mg,100-count bottles, Rx Only Manufactured by: Sandoz Inc., Princeton, NJ 08540 For BluePoint Laboratories, NDC 68001-223-00
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0260-2019·2018-11-21
Sandoz Recalls Isosorbide Dinitrate Tablets Due to Cross Contamination
Sandoz Inc. is recalling 5,100 bottles of Isosorbide Dinitrate Tablets, USP 10 mg, due to cross contamination with other products.
Product
Isosorbide Dinitrate Tablets, USP 10 mg,100-count bottles, Rx Only Manufactured by: Sandoz Inc., Princeton, NJ 08540 For BluePoint Laboratories, NDC 68001-225-00
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0369-2019·2018-11-21
GE Healthcare MyoSIGHT Nuclear Cardiology Imaging System Recall for Detaching Detector
GE Healthcare is recalling 276 Millennium MyoSIGHT Nuclear Cardiology Imaging Systems because a detector can detach and fall.
Product
GE Healthcare Millennium MyoSIGHT Nuclear Cardiology Imaging System H3000ZH Acquisition System
Category
Medical Device
Distribution
50 states
SevereFDA (Drugs)·D-0276-2019·2018-11-21
Taro Recalls Children's Allergy Solution Due to Impurity
Taro Pharmaceuticals is recalling 12,432 bottles of Children's 24 Hour Allergy Oral Solution because an unknown impurity exceeded limits during stability testing.
Product
Children's 24 Hour Allergy (cetirizine hydrochloride) Oral Solution 1 mg/mL, Bubble Gum Flavor, Sugar Free/Dye Free, 4 FL OZ (120 mL) bottle, Dist. by Meijer Distribution, Inc., Grand Rapids, MI 40644, NDC 41250-106-08, UPC 7 13733 88578 2.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0250-2019·2018-11-21
Kadesh Recalls Puriton Eye Relief Drops for Non-Sterility
Kadesh International is recalling Puriton Eye Relief Drops because they were manufactured under non-sterile production conditions.
Product
puriton EYE RELIEF DROPS, 0.5 oz (15 ml) bottle, Kadesh Inc., NDC#7079600115, UPC 7 36972 16799 0.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0450-2019·2018-11-21
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect
Zimmer Biomet is recalling 2,163 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Product
Affixus Hip Fracture Nail Left 125 Deg 9x165mm, Item Number 816709165 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullary hip screw to stabilize fractures of the proximal femur.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V825000·2018-11-21
Great Dane Recalls 2019 Freedom Trailers Due to Narrow Rear Impact Guards
Great Dane Trailers is recalling 2019 Freedom Combo Drop Deck Platform trailers because the rear impact guards may be too narrow, potentially failing to prevent vehicles from going under the trailer in a crash.
Product
GREAT DANE — GREAT DANE FREEDOM
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0460-2019·2018-11-21
Virtual Imaging RadPRO Mobile X-Ray System Recalled for Mount Separation Risk
Virtual Imaging is recalling 253 RadPRO Mobile 40kW Digital X-Ray Systems because the tube head may separate and fall off the unit.
Product
RadPRO(R) Mobile 40kW Digital X-Ray System - Model: SM-40HF-B-D-C Product Usage: Instrument is used to take diagnostic radiographic exposures of the skull, spinal column, chest, abdomen, extremities, and other body parts on both adult and pediatric subjects. Applications…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0438-2019·2018-11-21
Stryker Spirit Plus Bed Recall for Potential Entrapment Risk
Stryker is recalling 20,030 Spirit Plus hospital beds with high rail siderails due to non-compliance with safety standards and a potential risk of patient entrapment.
Product
The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option
Category
Medical Device
Distribution
50 states
HighFDA (Devices)·Z-0441-2019·2018-11-21
R82 A/S Recalls Heron Toilet and Bath Chairs Due to Aluminum Gas Spring
R82 A/S is recalling 687 Heron toilet and bath chairs because they contain aluminum gas spring heads. The recall is a replacement campaign for these specific units.
Product
Heron toilet and bath chair Model 880505-01 & 880505-11
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0258-2019·2018-11-21
Sandoz Recalls Isosorbide Dinitrate Tablets Due to Cross Contamination
Sandoz Inc. is recalling 18,832 bottles of Isosorbide Dinitrate 20 mg tablets due to cross-contamination with other products.
Product
ISOSORBIDE DINITRATE — ISOSORBIDE DINITRATE (ISOSORBIDE DINITRATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0451-2019·2018-11-21
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Malfunction
Zimmer Biomet is recalling 2,163 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Product
Affixus Hip Fracture Nail 125 Deg 10x165mm, Item Number 816710165 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullary hip screw to stabilize fractures of the proximal femur.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0445-2019·2018-11-21
Luminex Recalls Verigene Blood Culture Gram-Positive Nucleic Acid Kits
Luminex Corporation is recalling 12,700 trays of Verigene Blood Culture Gram-Positive Nucleic Acid Kits due to a potential for false negative results.
Product
VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as five-pack carriers) Product Usage: In vitro diagnostic test for the simultaneous detection and identification of potentially pathogenic gram-positive bacteria.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0469-2019·2018-11-21
Tosoh AIA-900 Analyzer Recalled Due to Pickup Arm Malfunction
Tosoh Bioscience is recalling 393 AIA-900 Analyzers because a pickup arm malfunction can stop the device from testing patient samples, causing delays in results.
Product
AIA-900 Analyzer, Product code 022930, 022930R
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0449-2019·2018-11-21
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect
Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Product
Affixus Hip Fracture Nail Left 130 Deg 11x300mm, Item Number 814611300 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullary hip screw to stabilize fractures of the proximal femur.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0452-2019·2018-11-21
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Issue
Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Product
Affixus Hip Fracture Nail 125 Deg 12x165mm, Item Number 816712165 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullary hip screw to stabilize fractures of the proximal femur.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0447-2019·2018-11-21
Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Issue
Zimmer Biomet is recalling 2,163 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Product
Affixus Hip Fracture Nail Left Deg 9x300mm, Item Number 814609300 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullary hip screw to stabilize fractures of the proximal femur.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0411-2019·2018-11-21
GE Healthcare Recalls Aisys Anesthesia Systems for Missing Backup Ventilation Feature
GE Healthcare is recalling Aisys anesthesia systems because a software upgrade prevents the device from automatically switching to backup ventilation if a patient stops breathing.
Product
Aisys Anesthesia System. Sold under the following product names: AISYS, AISYS 10.X TO 11.X UPGRADE KIT DUTCH, AISYS 10.X TO 11.X UPGRADE KIT ENGLISH, AISYS 10.X TO 11.X UPGRADE KIT ENGLISH FOR USA, AISYS 10.X TO 11.X UPGRADE KIT FRENCH, AISYS 10.X TO 11.X UPGRADE KIT GERMAN…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0453-2019·2018-11-21
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect
Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Product
Affixus Hip Fracture Nail 130 Deg 10x165mm, Item Number 816810165 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullary hip screw to stabilize fractures of the proximal femur.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0461-2019·2018-11-21
Medtronic Recalls Parietex Composite Parastomal Mesh Due to Failure Reports
Medtronic is voluntarily removing Parietex Composite Parastomal Mesh from the market after receiving reports of product failure leading to hernia recurrence.
Product
Parietex Composite Parastomal Mesh (Product Number PCOPM15 / PCOPM20) Product Usage: The PCOPM15 and PCOPM20 reorder codes are circular in shape, made from a three-dimensional monofilament polyester fabric with a two-dimensional monofilament polyester central band. One side…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0454-2019·2018-11-21
Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Issue
Zimmer Biomet is recalling 2,163 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Product
Affixus Hip Fracture Nail 130 Deg 12x165mm, Item Number 816812165 The Affixus Hip Fracture Nail System, comprised of short and long nails, provides surgeons with an intramedullary hip screw to stabilize fractures of the proximal femur.
Category
Medical Device
Distribution
Distributed nationwide