State

Rhode Island product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33226–33250 of 76790

HighFDA (Devices)·Z-0003-2020·2019-10-09
Metrix Secure EVA IV Bags Recalled for Potential Leaking
The Metrix Company is recalling 1,512 Secure EVA dual chamber IV bags due to a potential for leaking. The affected bags were distributed nationwide in the US.
Product
SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors, 4000mL, (legless) REF 66640 - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0002-2020·2019-10-09
Metrix Secure EVA Dual Chamber Container Recall for Leaking
The Metrix Company is recalling 4,284 Secure EVA dual chamber containers due to a potential for leaking. The affected bags are used for intravenous admixtures.
Product
SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors, 3000mL, (legless) REF 66630 - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0053-2020·2019-10-09
KRS Global Biotechnology Recalls Glutathione Vials Due to Sterility Concerns
KRS Global Biotechnology is recalling 402 vials of Glutathione 30 mL due to a lack of assurance of sterility. The product was distributed nationwide.
Product
Glutathione 30 mL Vial-For IM Use-Hypertonic solution, 6,000 mg/30 mL (200 mg/mL) Rx Only, KRS Global Biotechnology 791 Park of Commerce Blvd, Boca Raton, FL 33487. NDC3321674186
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0005-2020·2019-10-09
Metrix Secure EVA Dual Chamber IV Bags Recalled for Leaking
The Metrix Company is recalling 234,720 Secure EVA dual chamber IV bags due to a potential for leaking. The affected units were distributed nationwide in the US.
Product
SECURE EVA - DUAL CHAMBER CONTAINER with Manifold, 3000mL, REF 66631 (Canadian distribution) - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0062-2020·2019-10-09
KRS Global Biotechnology Recalls Hydroxocobalamin Vials Due to Sterility Concerns
KRS Global Biotechnology is recalling 345 vials of Hydroxocobalamin 10 mg/20 mL due to a lack of assurance of sterility. The recall covers all lots remaining within expiry and is distributed nationwide.
Product
Hydroxocobalamin 10 mg/20 mL (0.5 mg/mL) 20 mL fill in a 30 mL Vial, Rx Only, KRS Global Biotechnology 791 Park of Commerce Blvd, Boca Raton, FL 33487. NDC 3321678337
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0100-2020·2019-10-09
Sermorelin and GHRP-2 Lyophilized Vials Recalled Due to Sterility Concerns
KRS Global Biotechnology is recalling 120 vials of Sermorelin and GHRP-2 because the company cannot assure the products are sterile.
Product
Sermorelin, 3 mg / GHRP-2, 3 mg / Vial, For SC Use-Lyophilized, Rx Only, KRS Global Biotechnology 791 Park of Commerce Blvd, Boca Raton, FL 33487. NDC 3321674092
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0018-2020·2019-10-09
Implant Direct Sybron Recalls Mislabeled Dental Implant Vials
Implant Direct Sybron Manufacturing is recalling 22 vials of dental implants due to incorrect part numbers on the vial caps.
Product
ImplantDirect Legacy 3 Implant, REF 855216, SBM implant assembly, 2mmD x 16mmL, 4.5mmD platform, Rx, Sterile. The mislabeled model/part number on the vial cap is 835216. The responsible firm on the label is Implant Direct Sybron Manufacturing LLC, Thousand Oaks, CA.…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0119-2020·2019-10-09
Alkermes Recalls Vivitrol Kits Due to Needle Labeling Error
Alkermes is recalling 16,231 Vivitrol kits because 1-inch needles were incorrectly placed in sleeves labeled for 1.5-inch needles. The drug vials are not affected.
Product
VIVITROL — VIVITROL (NALTREXONE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2766-2019·2019-10-09
Roche Accu-Chek Performa II Meters Recalled for Damaged Capacitor
Roche Diabetes Care is recalling Accu-Chek Performa II meters because a damaged capacitor may cause short battery life or prevent the device from turning on.
Product
Accu-Chek Performa II Meter - Product Usage: a. The Accu-Chek Aviva Plus Blood Glucose Monitoring System is intended to be used for the quantitative measurement of glucose (sugar) in fresh capillary whole blood samples drawn from the fingertips, forearm, upper arm, or palm. The…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0001-2020·2019-10-09
Metrix Secure EVA Dual Chamber IV Bags Recalled for Leaking Risk
The Metrix Company is recalling 1,596 Secure EVA dual chamber IV bags due to a potential for leaking. The affected bags were distributed nationwide.
Product
SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors, 1500mL, (legless) REF 66615 - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2762-2019·2019-10-09
Zimmer Sidus Stem-Free Shoulder Humeral Head Recall for Incorrect Labeling
Zimmer GmbH is recalling 19 Sidus Stem-Free Shoulder Humeral Head implants due to incorrect size labeling on the packaging.
Product
Sidus Stem-Free Shoulder Humeral Head 50-18 Item number: 01.04555.500 orthopedic implant - Product Usage: The Sidus Stem-Free Shoulder is designed for long-term implantation into the human shoulder joint as a total shoulder arthroplasty in combination with Zimmer or Biomet s…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2763-2019·2019-10-09
Beckman Coulter Access Cortisol Reagent Recalled for Cross-Contamination
Beckman Coulter is recalling Access Cortisol Reagent due to cross-contamination that may cause falsely decreased patient results.
Product
The Access Cortisol Reagent. REF (Catalog Number) 33600, Lot 831755. A paramagnetic particle, chemiluminscent immunoassay. Product Usage: The assay is a paramagnetic particle, chemiluminescent immunoassay for the quanitative determination of cortisol levels in human serum…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2765-2019·2019-10-09
Roche Recalls Accu-Chek Aviva II Meters Due to Damaged Capacitor
Roche Diabetes Care is recalling 26,600 Accu-Chek Aviva II meters because a damaged capacitor may cause short battery life or prevent the device from turning on.
Product
Accu-Chek Aviva II Meter - Product Usage: a. The Accu-Chek Aviva Plus Blood Glucose Monitoring System is intended to be used for the quantitative measurement of glucose (sugar) in fresh capillary whole blood samples drawn from the fingertips, forearm, upper arm, or palm. The…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0066-2020·2019-10-09
Labetalol HCl syringes are recalled due to lack of sterility assurance
The FDA is recalling 6,405 units of Labetalol HCl single-dose syringes because there was insufficient assurance of sterility during production. No illnesses or injuries have been reported.
Product
Labetalol HCl 5 mg/mL 20 mg/4 mL (5 mg/mL) 4 mL Fill in a 6 mL Single Dose Syringe, Rx only, KRS Global Biotechnology 791 Park of Commerce Blvd, Boca Raton, FL 33487. NDC 3321676419
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0029-2020·2019-10-09
CooperSurgical Embryology Heated Plate Recall Due to Touchpad Malfunction
CooperSurgical is recalling 60 Embryology Heated Plates within the RI Witness system because the touchpad may not work properly after cleaning.
Product
Embryology Heated Plate within the RI Witness, Model Numbers 6-70-807, 6-70-807-A, & 6-70-807-B - Product Usage: RI Witness uses Radio Frequency Identification (RFID) to detect and monitor all activity in the IVF laboratory. The system helps mitigate the risk of human error…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2764-2019·2019-10-09
ELITech Viva-ProE Systems Recalled for Software Malfunction
ELITech Group B.V. is recalling 89 Viva-ProE Systems because a software malfunction causes the devices to become inoperable.
Product
Viva-ProE Systems, Model # 6003-670, UDI: 03661540600357 - Product Usage: The ELITech Clinical Systems Selectra ProM is an automated clinical chemistry system intended for use in clinical laboratories. It is intended to be used for a variety of assay methods that have been…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·19V716000·2019-10-08
2019 Mercedes-Benz and Freightliner Sprinter Door Component Recall
Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because an incorrectly installed door component may make doors harder to open after a severe frontal crash.
Product
MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 2500, SPRINTER 4500, SPRINTER 3500, SPRINTER 1500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·19V715000·2019-10-08
Mercedes-Benz Recalls Metris Vans Due to Exposed Battery Fire Risk
Daimler Vans USA is recalling 2016-2019 Mercedes-Benz Metris vehicles because the backup battery compartment may lack a cover, creating a fire hazard if conductive material contacts the terminals.
Product
MERCEDES-BENZ — MERCEDES-BENZ METRIS
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·20703·2019-10-08
Kawasaki Recalls Lawn Mower Engines Due to Burn and Fire Hazards
Kawasaki is recalling about 950 lawn mower engines because a fuel injector leak can cause burns or fires. No injuries have been reported.
Product
Lawn mower engines
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·20008·2019-10-08
IKEA Recalls MATVRÅ Infant Bibs Due to Choking Hazard
IKEA is recalling MATVRÅ infant bibs because the neck snaps can detach, posing a choking hazard to young children. No injuries have been reported.
Product
MATVRÅ Infant Bibs
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·20007·2019-10-08
Ronson Tech Torch Auto Start Recalled by Zippo Due to Fire Hazard
Zippo is recalling Ronson Tech Torch Auto Start lighters because they may continue to produce a flame after being turned off, posing a fire hazard.
Product
Ronson Tech Torch Auto Start
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·19V714000·2019-10-08
Thor Motor Coach Recalls Motorhomes with Incorrect Capacity Labels
Thor Motor Coach is recalling specific 2014-2020 motorhome models because incorrect carrying capacity labels may allow vehicles to be overloaded, increasing crash risk.
Product
THOR MOTOR COACH — THOR MOTOR COACH CITATION, SIESTA, QUANTUM, FOUR WINDS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·19V711000·2019-10-07
Freightliner Recalls 2018-2020 Cascadia Trucks for ABS Warning Light Defect
Daimler Trucks North America is recalling 2018-2020 Freightliner Cascadia trucks because the ABS warning light may fail to illuminate during low-voltage starts, potentially leaving drivers unaware of a malfunction.
Product
FREIGHTLINER — FREIGHTLINER CASCADIA
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·20702·2019-10-04
Mercane WideWheel Electric Scooters Recalled for Brake Failure and Injury Hazards
fluidfreeride is recalling Mercane WideWheel electric scooters because the brake caliper can fail, causing riders to lose control and suffer injuries.
Product
Mercane WideWheel Electric Kick Scooters
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·19V707000·2019-10-04
Blue Bird Recalls School Buses Due to Insufficient Roof Rivets
Blue Bird is recalling 2019-2021 school buses because insufficient roof rivets may allow roof sheets to separate in a crash, increasing injury risk.
Product
BLUE BIRD — BLUE BIRD VISION TRANSIT BUS, ALL AMERICAN SCHOOL BUS, VISION, VISION SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide