State

Connecticut product recalls

73,092 recalls have nationwide distribution and so reach Connecticut. 6,571 additional recalls listed Connecticut specifically in their distribution scope.

What the numbers show

Total: 6,571
Critical: 838
Severe: 1,590
Most recent: 2026-09-23

Of the 6,571 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 1,590 (24%) are Severe.

Which agencies issued them

These figures cover only the 6,571 recalls whose distribution notice names Connecticut specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9101–9125 of 79663

HighFDA (Food)·F-0155-2025·2024-12-04
Pancake and Griddle Mix Recalled for Potential Listeria Contamination
Multiple brands of griddle pancake and buttermilk mix made by Treehouse Foods are being recalled nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume the affected products.
Product
GIANT EAGLE 8/33oz GRDL PNCK BTRMLK - GT/EG UPC 030034071332 SCHNUCKS 8/33oz GRDL PNCK BTRMLK - SCHNK UPC 041318100020 SE GROCERS 8/33oz GRDL PNCK BTRMLK - SEGGR UPC 038259117170 BROOKSHIRE'S 8/33oz GRDL PNCK BTRMLK - BRKSH UPC 092825096740 SIGNATURE SELECT 8/33oz GRDL PNCK BTRML
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0063-2025·2024-12-04
Drug recall: Absorbine Jr. Ultra Strength Pain Patch manufacturing deviations
Absorbine Jr. Ultra Strength Pain Patch is being recalled nationwide due to manufacturing process deviations. The voluntary recall affects approximately 4,968,000 patches.
Product
ABSORBINE jr ULTRA STRENGTH PAIN PATCH, Menthol 6.5%, 1 patch per box, Distributed By: Absorbine Jr. LLC, Chattanooga, TN 37402 UPC 8 89476 41318 3, UPC 8 89476 41336 7
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0517-2025·2024-12-04
Discovery MR750w MRI Scanner Recalled for Elevated Acoustic Noise
GE Medical Systems is recalling 8 Discovery MR750w 3.0T MRI scanners because their gradient coils can produce elevated acoustic noise during scanning under specific conditions.
Product
Discovery MR750w 3.0T, whole body magnetic resonance scanner
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0179-2025·2024-12-04
Frozen Griddle and Belgian Waffle Products Recalled for Listeria Contamination Risk
Treehouse Foods is recalling multiple frozen griddle and Belgian waffle brands nationwide due to potential Listeria monocytogenes contamination. No illnesses have been reported.
Product
DUNCAN HINES 1/3.12kg GRDL WFL BLGN ORIG 4IN - DUNHN UPC 091479060275 KRUSTEAZ 1/3.44lb GRDL WFL BLGN ORIG - KRSTZ UPC 686151903331 KRUSTEAZ 1/3.44lb GRDL WFL BLGN ORIG-KRSMX UPC 00686151805307 KRUSTEAZ 1/3.44lb GRDL WFL BLGN ORIG - KRSTZ UPC 686151904017 GORDON CHOICE 1/3.12kg G
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0154-2025·2024-12-04
Breakfast Best Griddle Pancakes Recalled for Potential Listeria Contamination
Treehouse Foods is recalling Breakfast Best griddle pancakes nationwide due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and Best By dates between October 1, 2024 and October 11, 2025.
Product
BREAKFAST BEST 8/33oz GRDL PNCK BDAY-BKBST UPC 4061459959116
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0203-2025·2024-12-04
GOOD & GATHER griddle waffles recalled for potential Listeria contamination
GOOD & GATHER and 365 ORGANIC brand griddle waffles are being recalled due to potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and best-by dates from October 1, 2024 to October 11, 2025.
Product
GOOD & GATHER 12/9oz GRDL WFL MINI BLBRY ORG-GDGTR UPC 085239343012 365 ORGANIC 12/9oz GRDL WFL MINI BLBRY ORG - 365OR UPC 099482437008
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0157-2025·2024-12-04
Signature Select Griddle Pancakes Recalled for Potential Listeria Contamination
Treehouse Foods is recalling Signature Select Griddle Pancake Mini packages due to potential Listeria monocytogenes contamination. The recall involves 9,907,389 cases distributed across the United States and Canada.
Product
SIGNATURE SELECT 12/14.1oz GRDL PNCK MINI-SIGSL UPC 021130095889
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0537-2025·2024-12-04
Philips dS Breast 16ch 1.5T MRI Recalled for Patient Safety Risk
Philips North America is recalling approximately 5,231 dS Breast 16ch 1.5T MRI systems nationwide due to a potential safety issue that could harm patients during scan preparation or procedures.
Product
dS Breast 16ch 1.5T
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0161-2025·2024-12-04
H-E-B Griddle Waffles Recalled for Potential Listeria Contamination
Treehouse Foods is recalling H-E-B griddle waffles with blueberry and butter due to potential Listeria monocytogenes contamination. The recall affects approximately 9.9 million cases distributed nationwide.
Product
H-E-B 12/12.35oz GRDL WFL BLBRY-HEBUT UPC 041220008193
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0553-2025·2024-12-04
Shimadzu Autosampler Water Intrusion May Cause Electrical Short Circuit
Shimadzu laboratory autosamplers are being recalled due to water intrusion from a dehumidifier that can cause electrical short circuits. Affected units are distributed worldwide, including across the United States.
Product
Autosampler, Models: SIL-20ACXR CL, SIL-20ACHT CL, SIL-30AC CL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0511-2025·2024-12-04
MEDLINE ultrasound procedure kit connectors recalled due to insertion malfunction
Medline Industries is recalling procedure kits with connectors that may fail to open fully, preventing proper catheter insertion. The recall affects 3,396 units distributed in the U.S. and internationally.
Product
MEDLINE procedure kits labeled as follows: 1) ECHOSTIM BLOCK SET, REF DYNJRA9043S; 2) ULTRASOUND BLOCK PREP TRAY, REF PAIN1622A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0513-2025·2024-12-04
MEDLINE Epidural and Spinal Procedure Kits: Connector May Prevent Catheter Insertion
MEDLINE is recalling 3,744 epidural and spinal procedure kits due to a connector defect that may prevent proper catheter insertion. Affected kits were distributed nationwide and internationally.
Product
MEDLINE procedure kits labeled as follows: 1) CONT EPI 20G W/HUSTEAD, REF PAIN1069B; 2) CSE TRAY, REF PAIN1941; 3) TRAY CON EPID 20G NYL W/TUOHY, REF PAIN9023; 4) TRAY, CONT EPI 20G NYL W/ HUST, REF PAIN1281 5) TRAY, CONT EPI 20G NYL W/ HUST, REF PAIN9024
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0070-2025·2024-12-04
JR Watkins Menthol Pain Relief Patches Recalled for Manufacturing Deviations
JR Watkins Cooling Pain Relief Patches are being recalled due to manufacturing process deviations identified during production.
Product
JR WATKINS COOLING PAIN RELIEF PATCHES, Menthol 7.5%, 5 patches per box, Distributed By: J.R. Watkins, LLC, Oakland, CA 94612 UPC 8 56294 00878 5
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0558-2025·2024-12-04
Medline Endo Kit Recall: Missing Lot and Expiration Date Labels
Medline is recalling Endo Kit models containing Olympus components with missing sterile and manufacturing lot numbers and expiration dates on packaging. Without this labeling, medical facilities cannot verify product expiration or track inventory.
Product
ENDO KIT, Medline Kit SKU DYKE1577A, Component Number 57469, 10 per case; Medline Convenience Kits containing Single Use Biopsy Valve MAJ-1555
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0064-2025·2024-12-04
Absorbine Jr Pain Relieving Knee Patch recalled for manufacturing deviations
Unexo Life Sciences is recalling Absorbine Jr Pain Relieving Knee Patch nationwide due to manufacturing process deviations that do not meet FDA standards. No illnesses or injuries have been reported.
Product
ABSORBINE JR PAIN RELIEVING KNEE PATCH, Camphor 7%, Menthol 7%, packaged in a) 1 patch (UPC 8 89476 41251 3) and b) 6 patches (UPC 8 89476 41306 0), Distributed By: Absorbine Jr., LLC, Chattanooga, TN 37402
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0068-2025·2024-12-04
Equate Maximum Strength Lidocaine Pain Relieving Patches Recalled for Manufacturing Deviations
Equate Maximum Strength Lidocaine Pain Relieving Patches (4%) are being recalled due to current Good Manufacturing Practice deviations. Approximately 1.1 million patches were distributed nationwide in the US.
Product
EQUATE PAIN RELIEVING PATCHES — EQUATE PAIN RELIEVING PATCHES (LIDOCAINE 4%)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0062-2025·2024-12-04
Topical menthol back patch recalled for manufacturing deviations
ABSORBINE jr. Extra Large Back Patch containing 5% menthol is being recalled nationwide due to manufacturing compliance deviations. The Class II recall affects 6,848,820 patches distributed by Absorbine Jr., LLC.
Product
ABSORBINE jr. Extra Large BACK PATCH, Menthol 5%, 1 extra large patch per box, Distributed By: Absorbine Jr., LLC, Chattanooga, TN 37402 UPC 8 89476 41218 6, UPC 8 89476 41236 0
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0520-2025·2024-12-04
GE SIGNA and DISCOVERY PET/MR Scanners Recalled for Elevated Acoustic Noise
GE Medical Systems is recalling SIGNA PET/MR and DISCOVERY PET/MR imaging systems because gradient coils can produce elevated acoustic noise during scanning under specific conditions.
Product
Tomographic Imager Combining Emission Computed Tomography With Nuclear Magnetic Resonance: 1) SIGNA PET/MR, 2) DISCOVERY PET/MR,
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0065-2025·2024-12-04
THERACARE Lidocaine Pain Relief Patches Recalled for Manufacturing Deviations
THERACARE MAXIMUM STRENGTH PAIN RELIEF PATCH (4% lidocaine) is being recalled nationwide due to manufacturing practice deviations. Unexo Life Sciences, the manufacturer, voluntarily initiated the recall after identifying quality control issues.
Product
THERACARE MAXIMUM STRENGTH PAIN RELIEF PATCH — THERACARE MAXIMUM STRENGTH PAIN RELIEF PATCH (LIDOCAINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0552-2025·2024-12-04
Heart Device Transmitter Fails to Update Software After Power Interruption
Abbott Medical's Merlin@home transmitter cannot upgrade to current software after power interruptions during prior downloads. This affects remote heart device monitoring systems.
Product
Merlin@home with the MerlinOnDemand capability Transmitter REF EX1150 Merlin@home with the MerlinOnDemand" (MoD) capability is a transmitter configured for multiple patient use. It can receive information from an implantable heart device in unpaired mode. With MoD capability
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0075-2025·2024-12-04
Menthol pain relief patches recalled for manufacturing practice violations
J.R. Watkins is recalling Cooling Menthol Extra Strength Pain Relief Patches nationwide due to manufacturing practice deviations. The recall affects approximately 7,138 patches from lots JC101, JC102, and JC103.
Product
Cooling Menthol Extra Strength Pain Relief Patch, Menthol 7.5%, packaged in box of 5, Distributed by J.R. Watkins LLC, Oakland CA 94612 UPC 8 56294 00878 5, NDC 72342-100-05
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0551-2025·2024-12-04
Abbott Merlin@home Cardiac Monitoring Transmitters Fail to Update After Power Loss
Abbott is recalling 130 Merlin@home cardiac transmitters that cannot update software after power interruption during firmware download. Affected devices remain on outdated firmware with no ability to receive future updates.
Product
Merlin@home Transmitter REF EX1100 The Merlin@home" (M@h) transmitter is intended to transfer stored data from the patient s implanted heart device to Merlin.net" Patient Care Network (PCN) to facilitate remote monitoring by using inductive (EX1100 Model) or RF telemetry (E
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0072-2025·2024-12-04
Parche Leon pain relief patches recalled for manufacturing deviations
Unexo Life Sciences Private Limited is voluntarily recalling Parche Leon pain relief patches due to manufacturing practice deviations. No illnesses or injuries have been reported.
Product
PARCHE LEON — PARCHE LEON (CAPSAICIN, CAMPHOR, MENTHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0554-2025·2024-12-04
Shimadzu Autosampler Devices Subject to Water Damage Affecting Main Board
Water condensation may accumulate under the autosampler's thermal insulation and damage the main board, causing communication errors and delays in laboratory testing. Two Shimadzu models are affected: SIL-40C XR CL and SIL-40C X3 CL.
Product
Autosampler, Models: SIL-40C XR CL, SIL-40C X3 CL
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0066-2025·2024-12-04
FDA Recalls Menthol Medicated Patches Due to Manufacturing Deviations
FDA recalls THERA CARE COLD HOT MEDICATED PATCH (menthol 5%) due to manufacturing practice deviations. The voluntary recall affects 279,936 patches distributed nationwide.
Product
THERA CARE COLD HOT MEDICATED PATCH — THERA CARE COLD HOT MEDICATED PATCH (MENTHOL)
Category
Drug
Distribution
Distributed nationwide