State

Colorado product recalls

73,096 recalls have nationwide distribution and so reach Colorado. 6,944 additional recalls listed Colorado specifically in their distribution scope.

What the numbers show

Total: 6,944
Critical: 1,218
Severe: 1,509
Most recent: 2026-09-23

Of the 6,944 recalls naming Colorado we have scored against our rubric, 1,218 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,509 (22%) are Severe.

Which agencies issued them

These figures cover only the 6,944 recalls whose distribution notice names Colorado specifically. The 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9151–9175 of 80040

HighFDA (Devices)·Z-0532-2025·2024-12-04
Medline Surgical Kits Recalled for Incorrect Needle and Suture Specifications
Medline Industries is recalling 408 surgical kits from Alabama, Georgia, Massachusetts, New Jersey, and Pennsylvania. Some suture packages within the kits contain incorrect needle types and sizes, and incorrect suture diameters and lengths.
Product
(1) Medline Open Heart CDS, REF CDS840132O, packaged 1 kit/case, non-sterile; and (2) Medline Dr. Davies CV, REF DYNJ903016G, packaged 1 kit/case, non-sterile.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0170-2025·2024-12-04
Multiple Store-Brand Griddle Waffles Recalled for Potential Listeria Contamination
Treehouse Foods is recalling approximately 9.9 million cases of frozen griddle waffles with blueberries distributed nationwide in the USA and Canada due to potential Listeria monocytogenes contamination.
Product
PRESIDENT'S CHOICE 12/320g GRDL WFL BLBRY GF-PCHOI UPC 060383038663 WILD HARVEST 12/11.3oz GRDL WFL BLBRY GF-WLDHR UPC 711535515173 WEGMANS 12/11.3oz GRDL WFL BLBRY GF-WEGMN UPC 077890519653 FULL CIRCLE 12/11.3oz GRDL WFL BLBRY GF-FULLC UPC 036800486980 FOODHOLD 12/11.3oz GRDL WF
Category
Food
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-0156-2025·2024-12-04
Treehouse Foods Griddle Pancakes Recalled for Potential Listeria Contamination
SE Grocers and Pics by Price Chopper brand griddle pancakes are being recalled by Treehouse Foods due to potential Listeria monocytogenes contamination. Affected products were distributed nationwide in the USA and Canada.
Product
SE GROCERS 12/16.5oz GRDL PNCK HSTYLE-SEGGR UPC 038259117194 PICS BY PRICE CHOPPER 12/16.5oz GRDL PNCK HSTYLE-PRCHP UPC 041735157386
Category
Food
Distribution
Distributed nationwide
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 (Food)·F-0163-2025·2024-12-04
Treehouse Foods Frozen Griddle and Blueberry Waffles Recalled for Listeria Risk
Treehouse Foods is recalling multiple store-brand frozen waffles nationwide for potential Listeria monocytogenes contamination. The recall affects products with batch codes starting with 2C and best-by dates from October 1, 2024 to October 11, 2025.
Product
PICS BY PRICE CHOPPER 6/29.6oz GRDL WFL BB - PRCHP UPC 041735089656 NO NAME 1/1.68kg GRDL WFL BB - NNAME UPC 060383987732 NO NAME 12/280g GRDL WFL BB - NNAME UPC 060383987671 WESTERN FAMILY 12/280g GRDL WFL BLBRY - WSTCN UPC 062639335861 GREAT VALUE 12/280g GRDL WFL BB - GRVLC UP
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0200-2025·2024-12-04
Griddle Waffles Recalled for Potential Listeria Contamination
Treehouse Foods is recalling approximately 9.9 million cases of Krusteaz griddle waffles and related products due to potential Listeria monocytogenes contamination. Products with batch codes starting with 2C and best-by dates through October 11, 2025 are included.
Product
KRUSTEAZ 1/2.5lb GRDL WFL BLGN 7-KRSTZ UPC 068615115168 KRUSTEAZ 1/11.25oz GRDL WFL BLGN-KRSTZ UPC BAKERS SOURCE 1/11.25oz GRDL WFL BLGN-BKRSC UPC 089356143562 GORDON FOOD SERVICE 3/2.5lb GRDL WFL BLGN 7-GDNFS UPC 093901310323
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0536-2025·2024-12-04
Philips Achieva TX Interventional Coil 3.0T Recalled for Patient Safety Risk
Philips recalls the Achieva TX Interventional Coil 3.0T (5,231 units) for a potential safety issue that may harm patients during MRI scan preparation or procedures.
Product
Achieva TX Interventional Coil 3.0T
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0166-2025·2024-12-04
Nature's Path Organic Griddle Waffles Recalled for Potential Listeria Contamination
Treehouse Foods is recalling Nature's Path Organic Griddle Waffles (9,907,389 cases) for potential Listeria monocytogenes contamination. Affected products have batch codes starting with 2C and Best By dates from October 1, 2024 through October 11, 2025.
Product
NATURES PATH ORGANIC 12/7.4oz GRDL WFL BCKWHE BRY ORG GF-NPTHO UPC 058449590583 NATURES PATH ORGANIC 12/210g GRDL WFL BCKWHE BRY ORG GF-NPOCN UPC 058449590576
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0186-2025·2024-12-04
Treehouse Foods recalls Nature's Path organic griddle waffles for Listeria contamination risk
Treehouse Foods is recalling Nature's Path Organic griddle waffles due to potential Listeria monocytogenes contamination. The affected products were distributed nationwide in the United States and Canada.
Product
NATURES PATH ORGANIC 12/7.4oz GRDL WFL CHOC CHIP ORG GF-NPTHO UPC 058449167013 NATURES PATH ORGANIC 12/210g GRDL WFL CHOC CHIP ORG GF-NPOCN UPC 058449167006
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0510-2025·2024-12-04
Medline Epidural Catheter Kits Recalled Due to Connector Position Defect
Medline is recalling over 5,900 epidural catheter kits because the connectors may not open fully, preventing proper catheter insertion. The recall affects units distributed nationwide and internationally.
Product
MEDLINE procedure kits labeled as follows: 1) 20G EPI CATH SINGLE STERILE, REF EPICATH19 2) 20G EPI CATH SINGLE STERILE, REF EPICATH20
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
HighFDA (Devices)·Z-0508-2025·2024-12-04
Medline Nexus Catheter Connectors May Fail to Open Properly
Medline recalls 1,975 NEXUS catheter connectors that may not fully open, preventing proper catheter insertion. Affected units were distributed nationwide and internationally.
Product
MEDLINE NEXUS 19/20G CATH CONNECTOR, Medline SKU REF NEXCONNECT, Catheter Connector
Category
Medical Device
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-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 (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-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
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 (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-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-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-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 (Drugs)·D-0071-2025·2024-12-04
FDA Recalls Cheeky Bonsai Menthol Pain Relief Patches for Manufacturing Deviations
Cheeky Bonsai Pain Relief Patches (Menthol 10%) are being recalled nationwide due to manufacturing facility compliance deviations. The voluntary recall affects 17,928 patches distributed across the US.
Product
CHEEKY BONSAI PAIN RELIEF PATCHES, Menthol 10%, 4 patches per box, Distributed by Cheeky Bonsai, San Francisco, CA UPC 8 60006 57564 9
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0069-2025·2024-12-04
LILAS Feminine Pain Relief Patch recalled for manufacturing violations
Unexo Life Sciences is voluntarily recalling LILAS Feminine Pain Relief Patch nationwide due to manufacturing practice deviations affecting 363,300 patches.
Product
LILAS Feminine Pain Relief Patch, Menthol 10%, a) 5 patches per box (UPC 7 87099 48212 1) and 10 patches per box (UPC 7 87099 48211 4), Distributed by: Lilas Wellness, Inc., Beaverton, Oregon 97008-7105
Category
Drug
Distribution
Distributed nationwide