State

Connecticut product recalls

73,584 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 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25751–25775 of 80156

HighFDA (Devices)·Z-2540-2021·2021-09-29
C.R. Bard Foley Catheter Care Kits Recalled for Potential Sterile Barrier Defect
C.R. Bard Inc is recalling Foley catheter care kits (catalog A303416A) because potential packaging defects could compromise the sterile barrier. Approximately 6,440 units were distributed nationwide.
Product
Catalog A303416A, SureStep" Foley Tray, Lubri-Sil" I.C., Temperature Sensing Complete Care", Drainage Bag, StatLock" Stabilization Device
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2498-2021·2021-09-29
cobas SARS-CoV-2 and Influenza A/B Test Recalled Due to False Positive Results
Roche Molecular Systems is recalling cobas SARS-CoV-2 & Influenza A/B test kits following reports of increased false positive SARS-CoV-2 results.
Product
cobas SARS-CoV-2 & Influenza A/B Test for use on the cobas Liat System, Catalog Number 09211101190
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V758000·2021-09-29
2022 GMC Sierra brake modulator assembly bolts may fail to seal
General Motors is recalling 2021-2022 Chevrolet Silverado and GMC Sierra pickup trucks due to brake modulator bolts that may fail to seal properly. Water intrusion can cause electrical short circuits, creating a fire risk.
Product
CHEVROLET — CHEVROLET, GMC SILVERADO 3500, SIERRA 2500, SIERRA 3500, SILVERADO 2500
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·21202·2021-09-29
Martha Stewart Collection Oil & Vinegar Cruets Recalled for Laceration Hazard
Macy's is recalling Martha Stewart Collection Oil & Vinegar Cruets because the glass portion can break during use, causing cuts. Six incidents have been reported, including three lacerations with two requiring stitches.
Product
Martha Stewart Collection Oil & Vinegar Cruets
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2497-2021·2021-09-29
Bronchofibervideoscope recalled for potential leak in insertion tube
Olympus is recalling the EVIS EXERA BF-XT160 bronchofibervideoscope due to a missing gluing step in manufacturing. The affected devices may develop leaks in the insertion tube, posing an infection control risk.
Product
EVIS EXERA BF-XT160 Bronchofibervideoscope, Model No. BF-XT160
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21203·2021-09-29
Venom Motorsports Youth ATVs Recalled Due to Crash and Safety Standard Violations
Venom Motorsports is recalling about 500 youth all-terrain vehicles (ATVs) because they do not meet mandatory safety requirements, including speed restrictions, and were distributed without CPSC approval. The recalled ATVs pose a risk of serious injury or death.
Product
Venom Youth All-Terrain Vehicles (ATVs)
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2517-2021·2021-09-29
Sight OLO-E1/U1 Reference Range Labeling Discrepancy in Software
The Sight OLO-E1/U1 diagnostic device software contains a labeling discrepancy: the operator's manual and software present different adult CBC reference ranges, potentially affecting the interpretation of diagnostic results.
Product
Sight OLO-E1/U1 Software and Operators Manual Software v2.56.1 Catalog #: 1 OLO-U1 Catalog #: 2 OLO-E1 revision 1.9, revision 1.10
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2533-2021·2021-09-29
Foley Catheter Tray Packaging Defect Poses Sterile Barrier Risk
C.R. Bard Inc is recalling a Foley catheter tray due to potential packaging defects that may compromise the sterile barrier. Approximately 1,710 units were distributed nationwide.
Product
Catalog A897514, SureStep" Foley Tray, Silicone, Drainage Bag, StatLock" Stabilization Device
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2511-2021·2021-09-29
Univation X System knee implants recalled for loosening risk
Aesculap Implant Systems is recalling Univation X System knee implants because they may loosen, potentially requiring additional surgery. The recall affects devices distributed nationwide.
Product
Univation X System knee implant devices as follows: Catalog/Product: NL482 UNIVATION F MENISCAL COMP.T1 RM/LM 9MM; NL483 UNIVATION F MENISCAL COMP.T2 RM/LM 9MM; NL484 UNIVATION F MENISCAL COMP.T3 RM/LM 9MM; NL485 UNIVATION F MENISCAL COMP.T4 RM/LM 9MM; NL486 UNIVATION F…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2527-2021·2021-09-29
C.R. Bard SureStep Foley Catheter Tray Sterile Barrier Defect Recall
C.R. Bard is recalling 5,950 SureStep Foley Tray kits nationwide due to potential packaging defects that may impact the sterile barrier.
Product
Catalog A319416AM, SureStep" Foley Tray, Bardex" I.C., Complete Care", Urine Meter, Temperature Sensing, StatLock" Stabilization Device
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2512-2021·2021-09-29
Univation X Knee Implant Devices Recalled Due to Loosening Risk
Aesculap Implant Systems is recalling Univation X System knee implant devices (all lots, nationwide) because the implants may loosen, potentially requiring revision surgery. No injuries have been reported.
Product
Univation X System knee implant devices as follows: Catalog/Product: NL488 UNIVATION F MENISCAL COMP.T1 RM/LM 10MM; NL489 UNIVATION F MENISCAL COMP.T2 RM/LM 10MM; NL490 UNIVATION F MENISCAL COMP.T3 RM/LM 10MM; NL491 UNIVATION F MENISCAL COMP.T4 RM/LM 10MM; NL492 UNIVATION…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2507-2021·2021-09-29
Greiner VACUETTE 2 ml Coagulation Blood Collection Tubes Anticoagulant and Vacuum Recall
Greiner Bio-One is recalling 956,400 VACUETTE coagulation blood collection tubes that may clot due to anticoagulant variation or low vacuum.
Product
Greiner Bio-One VACUETTE¿ TUBE 2 ml 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube, non-ridged
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2529-2021·2021-09-29
Foley Catheter Tray Recalled Due to Potential Packaging Defects
C.R. Bard is recalling 2,660 units of SureStep Foley Catheter Trays nationwide due to potential packaging defects that may impact the sterile barrier.
Product
Catalog A800061, SureStep" Foley Tray, Bard LubricathTM Foley Catheter Tray
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2521-2021·2021-09-29
C.R. Bard SureStep Foley Tray Recalled for Packaging Defect Risk
C.R. Bard is recalling SureStep Foley Tray units due to potential packaging defects that may compromise the sterile barrier. The recalled product was distributed nationwide in the United States.
Product
Catalog A119216M, SureStep" Foley Tray, Lubri-Sil", Urine Meter, Temperature Sensing Dual, StatLock" Stabilization Device
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0812-2021·2021-09-29
Metoprolol Tartrate Tablets Recalled for Metal Wire Contamination
Aurobindo Pharma USA Inc. is recalling Metoprolol Tartrate 100 mg tablets due to the presence of metal wire found in at least one tablet. The FDA classified this as a Class II recall affecting 2,820 bottles distributed nationwide.
Product
METOPROLOL TARTRATE — METOPROLOL TARTRATE (METOPROLOL TARTRATE)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·21V769000·2021-09-29
Class A motorhomes recalled for instrument cluster blanking while in motion
Jayco is recalling certain 2019-2021 Entegra and Jayco Class A motorhomes because the instrument cluster may go blank while driving, potentially hiding speed and warning lights.
Product
JAYCO — JAYCO, ENTEGRA EMBARK, ANTHEM, ASPIRE, CORNERSTONE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2535-2021·2021-09-29
SureStep Foley Tray Recall: Packaging Defects May Compromise Sterile Barrier
C.R. Bard Inc is recalling SureStep Foley Trays (Catalog A902616) due to packaging defects that may compromise the sterile barrier. Affected units were distributed nationwide.
Product
Catalog A902616, SureStep" Foley Tray, Bardex" I.C., Lubricath", Urine Meter
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2501-2021·2021-09-29
Scorpion Portal Vein Access Set Recalled for Cracking Sheaths
Argon Medical Devices is recalling the Scorpion Portal Vein Access Set due to design changes that have caused the sheaths to crack or break at the tips. The affected product was distributed in the United States.
Product
Scorpion Portal Vein Access Set - Product Usage: used to gain access to the hepatic vein and guide a sharp puncture tool (0.040 Stylet or 17ga Needle) through the parenchyma.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2494-2021·2021-09-29
Ad-Tech Medical Cable Recalled Due to Incorrect Product Labels
Ad-Tech Lightweight CABRIO Cables with incorrect labels are being recalled. Mislabeling could cause product misidentification affecting proper use in clinical monitoring applications.
Product
Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0809-2021·2021-09-29
Pfizer recalls Chantix tablets for N-nitroso-varenicline impurity
Pfizer is recalling certain lots of Chantix (varenicline tartrate) 0.5mg tablets nationwide due to the presence of N-nitroso-varenicline impurity above FDA's acceptable interim intake limit.
Product
CHANTIX — CHANTIX (VARENICLINE TARTRATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2495-2021·2021-09-29
Ad-Tech TECH ATTACH Cable Recalled for Incorrect Label Information
Ad-Tech Medical recalled its Lightweight TECH ATTACH Cable due to incorrect labels on affected units. The cables are designed to connect electrodes to third-party monitors and stimulators.
Product
Ad-Tech Lightweight TECH ATTACH Cable - Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0813-2021·2021-09-29
Sirolimus Tablets Recalled for Failed Impurities and Degradation Specifications
American Health Packaging is recalling Sirolimus 1 mg tablets (Lot #1000789, expiring 10/31/2022) distributed nationwide because they failed impurities and degradation specifications.
Product
SIROLIMUS — SIROLIMUS (SIROLIMUS)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0823-2021·2021-09-29
Drug Recall: Chlorzoxazone Tablets Due to Manufacturing Deviations
Glenmark Pharmaceuticals is recalling 1,800 bottles of Chlorzoxazone Tablets USP 375 mg nationwide due to current Good Manufacturing Practice (CGMP) deviations. The recall was initiated on August 27, 2021.
Product
Chlorzoxazone Tablets USP 375 mg 100 Tablets Rx Only NDC 68462-724-01 Manufactured by: Glenmark Pharmaceuticals Inc., USA 4147 Goldmine Road Monroe, NC 28110 Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0828-2021·2021-09-29
Betadine Povidone-Iodine Solution Swabstick recalled for subpotent drug
Avrio Health L.P. is recalling Betadine Solution Swabstick in single and three-count packages nationwide because the product is subpotent—meaning it contains less active ingredient than specified. Consumers should stop using affected lots and consult their healthcare provider if needed.
Product
BETADINE — BETADINE (POVIDONE-IODINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0808-2021·2021-09-29
Chantix Varenicline Tablets Recalled for Nitroso Impurity
Pfizer is recalling Chantix (varenicline) tablets nationwide due to the presence of N-nitroso-varenicline impurity above FDA's acceptable interim intake limit, a manufacturing deviation.
Product
Chantix (varenicline) tablets 0.5mg/1mg, 56 Tablets, Rx only, Distributed by Pfizer Labs, Division of Pfizer Inc. NY, NY 10017, Made in Ireland, NDC 00069-0471-03. carton containing one blister pack of 11 0.5 mg tablets and one blister pack containing 42.1 mg tablets.
Category
Drug
Distribution
Distributed nationwide