State

Connecticut product recalls

73,509 recalls have nationwide distribution and so reach Connecticut. 6,572 additional recalls listed Connecticut specifically in their distribution scope.

What the numbers show

Total: 6,572
Critical: 838
Severe: 1,881
Most recent: 2026-10-14

Of the 6,572 recalls naming Connecticut we have scored against our rubric, 838 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,881 (29%) are Severe.

Which agencies issued them

These figures cover only the 6,572 recalls whose distribution notice names Connecticut specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23501–23525 of 80081

SevereCPSC·22094·2022-03-09
Olight M2R Pro and Warrior Mini Flashlights Recalled for Burn Hazard
Olight is recalling about 215,100 M2R Pro and Warrior Mini flashlights because they can turn on accidentally and overheat while stored in a holster or pocket, creating a burn hazard. The company has received 127 reports of unintended activation with 22 burn injuries, including three second-degree burns.
Product
M2R Pro and Warrior Mini Flashlights
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0720-2022·2022-03-09
BUTLER Clear Dip Recalled for Lack of FDA Premarket Clearance
Sunstar Americas is recalling BUTLER Clear Dip nationwide due to lack of FDA premarket clearance. The product was distributed in 22,514 units across multiple lot codes.
Product
BUTLER Clear Dip, 12 bottles/case
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0689-2022·2022-03-09
Titanium Toe Joint Implant Labeling Error: Unvalidated MRI Safety Claims
BioPro Titanium MPJ toe implants are recalled due to false documentation claiming MRI safety testing that was never performed. Patients should not undergo MRI with this implant until properly evaluated.
Product
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC LG, Part ID 17038
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0721-2022·2022-03-09
Surgical knee navigation implant recalled over sterilization failures
Orthosoft's NavitrackER knee navigation system may lack proper sterilization. The product was distributed without passing required sterilization tests, risking infection.
Product
NavitrackER Kit A: Knee, Model Number 20-8000-000-07,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0688-2022·2022-03-09
Titanium Toe Joint Implant Contains False MR Compatibility Claims
BioPro recalled titanium toe implants due to incorrect claims in documentation about magnetic resonance (MR) compatibility testing that was never conducted. The FDA issued a Class II recall to address the misleading safety information.
Product
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC M/L, Part ID 17037
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0699-2022·2022-03-09
Helix Elite Molecular Reference Standard Recall for Failed Shelf-Life Testing
Microbiologics Inc is recalling Helix Elite Molecular Standards for inactivated RSV A because real-time shelf life testing failed at 24 months, indicating the product may not maintain stability through its claimed expiration date.
Product
Helix Elite" Molecular Standards: Inactivated Standard. Inactivated Respiratory Syncytial Virus A Strain Long. Target pathogens are lyophilized in a PCR compatible matrix, and stable at 2¿C-25¿C through the expiration date. Each lyophilized pellet is packaged in a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0712-2022·2022-03-09
KWIK-STIK Quality Control Kit Recalled for Incorrect Antibiotic Susceptibility
Microbiologics Inc is recalling KWIK-STIK quality control kits containing Enterococcus faecalis because certain lots are susceptible to Gentamicin Synergy when they should be resistant. The defect could affect laboratory testing accuracy.
Product
KWIK-STIK, Quality control kit for culture media, sold as: a. KWIK-STIK 2-pack Enterococcus faecalis derived from ATCC 51299 b. KWIK-STIK 6-pack Enterococcus faecalis derived from ATCC 51299
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0715-2022·2022-03-09
Stryker medical implant recalled for manufacturing defect in barrier layer
Stryker is recalling MEDPOR Titan OFW implants after one unit was found with an incorrectly placed barrier layer. The defect resulted from manufacturing error rather than design.
Product
MEDPOR Titan OFW - MTB - Right - 1.0mm, Catalog number 81032
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0710-2022·2022-03-09
Abbott Alinity m reaction units risk detachment during transport
Abbott Molecular is recalling 3063 kits of Alinity m Integrated Reaction Units due to potential detachment of reaction vessels from the unit cap during transport. No injuries have been reported.
Product
Alinity m Integrated Reaction Units (IRU)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0702-2022·2022-03-09
da Vinci Surgical Cannula Reducer Metal Tip May Dislodge During Surgery
Intuitive Surgical is recalling the da Vinci Xi and X 12-8 mm Conductive Cannula Reducer because the metal tip may dislodge from the plastic shaft. If unnoticed, additional surgery may be needed, or energy leakage could cause tissue damage.
Product
da Vinci Xi and X 12-8 mm Conductive Cannula Reducer, REF: 470381-11
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0686-2022·2022-03-09
Titanium Toe Implants Recalled for Incorrect MRI Safety Labeling
BioPro Titanium MPJ toe implants are recalled because labeling incorrectly claims MRI safety without actual testing. Patients should consult their physician before undergoing MRI procedures.
Product
Titanium MPJ (Toe Implant)TOE JOINT TITANIUM PC SM, Part ID 17035
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0691-2022·2022-03-09
Titanium MPJ Toe Implant Recalled for Incorrect MR Safety Labeling
BioPro is recalling Titanium MPJ toe implants (Lot 125651) with inaccurate labeling claiming MR compatibility when the implant has not been tested for magnetic resonance safety. Patients should consult their physician before MRI.
Product
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MS, Part ID 17198
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0696-2022·2022-03-09
MEDLINE Micro-Kill Bleach Germicidal Wipes Recall: Out-of-Specification Sodium Hypochlorite
MEDLINE recalls Micro-Kill Bleach Germicidal Wipes due to out-of-specification low levels of sodium hypochlorite, the active disinfecting ingredient. Affected batches may have reduced effectiveness.
Product
MEDLINE Micro-Kill Bleach Germicidal Bleach Wipes
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0681-2022·2022-03-09
Acorn stairlifts recalled due to inadequate seat structural strength
Acorn Stairlifts Inc. is recalling multiple stairlift models because the seats may not have adequate strength to consistently support users during continued use, creating a fall hazard.
Product
Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0700-2022·2022-03-09
Helix Elite Molecular Standard Fails FDA Shelf-Life Stability Testing
Microbiologics Inc. recalls Helix Elite Inactivated Neisseria gonorrhoeae Strain GL0071 molecular standard after real-time shelf life testing failed at 24 months. The product was distributed nationwide and internationally.
Product
Helix Elite" Molecular Standards: Inactivated Standard. Inactivated Neisseria gonorrhoeae Strain GL0071.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22096·2022-03-09
Honda Talon 1000 ROVs recalled for engine failure and crash risk
Honda is recalling approximately 32,000 Talon 1000 recreational off-highway vehicles from 2019-2021 because a loose intake funnel band screw can enter the engine and cause sudden failure, potentially leading to loss of control and crashes.
Product
Honda Talon 1000 ROVs
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0687-2022·2022-03-09
Titanium Toe Implant Recalled for Incorrect MRI Safety Claims
BioPro Titanium MPJ toe implant documentation incorrectly claims MRI safety testing that was never conducted. The implant is not proven safe for MRI use.
Product
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MD, Part ID 17036
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0690-2022·2022-03-09
Titanium Toe Implant Recalled for Incorrect MRI Safety Statements
BioPro is recalling Titanium MPJ toe implants due to false claims of MRI compatibility. The device instruction manual states it is MRI-safe despite not being tested.
Product
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MS, Part ID 17197
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0711-2022·2022-03-09
Bronchial Microbiology Brush Labeling Error—Cleared Only for Gastrointestinal Use
Hobbs Medical is recalling 38,357 Bronchial Microbiology Brushes due to labeling that incorrectly indicates bronchial use. The device is cleared only for gastrointestinal use.
Product
Bronchial Microbiology Brush, Catalog Number 4310 and 4320. Microbial sampling is performed by compressing a spring as the base of brush wire to expose the brush, scraping the desired surface, and releasing the compression on the spring which retracts the brush back into the…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0706-2022·2022-03-09
K2M Everest MI XT Outer Dilators recalled for manufacturing defect
K2M is recalling 686 Everest MI XT Outer Dilator units due to a manufacturing nonconformance that prevents them from fitting properly with inner dilators during surgical procedures.
Product
Everest MI XT Outer Dilator, Catalog Number 5101-90168
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0705-2022·2022-03-09
K2M Everest MI XT Inner Dilator Recalled for Manufacturing Fit Defect
K2M recalled 686 units of the Everest MI XT Inner Dilator due to a manufacturing nonconformance preventing proper fit with outer dilators during surgery. Two complaints prompted the recall.
Product
Everest MI XT Inner Dilator, Catalog Number 5101-90167
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0684-2022·2022-03-09
BioPro Titanium MPJ Toe Implant MRI Safety Labeling Error
BioPro is recalling Titanium MPJ toe implants due to false MRI safety labeling. The instructions and patient cards incorrectly state the device was tested for MRI safety, but no testing was conducted.
Product
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC ML, Part ID 16815
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0708-2022·2022-03-09
OPAQUE Lacrimal Plugs recalled due to sterile pouch seal defect
Lacrimedics is recalling approximately 5,767 units of OPAQUE Lacrimal Plugs due to potential defects in the sterile pouch seal that could compromise product sterility. The affected devices were distributed nationwide and internationally.
Product
OPAQUE Herrick Lacrimal Plugs, HP3, 0.3 mm, HP5, 0.5mm, HP7, 0.7.mm, STERILE, EO, Rx only, CE Dry eye treatment
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0698-2022·2022-03-09
QC Control Panels Fail Shelf Life Stability Test at 24 Months
Microbiologics QC control panels for bacterial diagnostic testing failed shelf life validation at 24 months. The 29 affected units were distributed across US states and internationally to Canada, UK, Australia, Belgium, and India.
Product
Microbiologics QC Sets and Panels. BD MAX" CT/GC/TV Verification and Control Panel. Containing High, Medium and Low Level Controls.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22093·2022-03-09
Danby Free-Standing and Slide-In Ranges Recalled for Tip-Over Hazard
Danby is recalling about 1,700 free-standing and slide-in electric and gas ranges because the anti-tip-over bracket may not be securely installed, creating a tip-over hazard and risk of burn injuries when heavy objects are placed on an open oven door.
Product
Danby brand free-standing and slide-in electric and gas ranges
Category
Consumer Product
Distribution
Distributed nationwide