State

Colorado product recalls

73,219 recalls have nationwide distribution and so reach Colorado. 6,945 additional recalls listed Colorado specifically in their distribution scope.

What the numbers show

Total: 6,945
Critical: 1,218
Severe: 1,510
Most recent: 2026-10-02

Of the 6,945 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 1,510 (22%) are Severe.

Which agencies issued them

These figures cover only the 6,945 recalls whose distribution notice names Colorado specifically. The 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

15251–15275 of 80164

HighFDA (Devices)·Z-2606-2023·2023-09-27
DJO Surgical Reverse Shoulder System Components Recalled Due to Missing Sterilization
Reverse shoulder implant components were shipped without final sterilization, potentially leading to infection and possible revision surgery if implanted. Encore Medical is recalling 64 units distributed across the US and internationally.
Product
DJO Surgical: Reverse Shoulder System (RSP) Semi Humeral Socket Insert, 32mm, REF: 508-01-032; Baseplate, Glenoid HA-Coat, RSP, 6.5mm X 30mm, REF: 508-32-104; Reverse Shoulder System (RSP) Glenoid, Neutral Head W/ Retaining Screw, 36mm, REF: 508-36-101
Category
Medical Device
Distribution
26 states
HighFDA (Drugs)·D-1165-2023·2023-09-27
TRP Natural Eyes Stye Relief sterile eye ointment recalled for lack of sterility assurance
FDA is recalling TRP Natural Eyes Stye Relief sterile eye ointment due to lack of assurance of sterility. The product was distributed to two accounts in Rhode Island and Colorado.
Product
TRP Natural Eyes, Stye Relief, Sterile Eye Ointment, Homeopathic 0.14 oz (4 grams), Manufactured in Jordan, exclusively for TRP Company, Inc., 1575 Delucchi Lane, Reno, NV 89502, NDC: 17312-014-13.
Category
Drug
Distribution
2 states
HighFDA (Drugs)·D-1175-2023·2023-09-27
Humanrace Suncare SPF 30 Sunscreen Recalled for Subpotent Protection
HUMANRACE is recalling Humanrace Suncare Ozone Face Protection Daily Moisturizer SPF 30 because the product does not contain the declared SPF level. Affected consumers should discontinue use immediately.
Product
Humanrace Suncare, Ozone Face Protection Daily Moisturizer, Broad Spectrum Sunscreen SPF 30, packaged as a 53mL (1.8 fl oz.) bottle, 100% mineral, Active Ingredient: Zinc oxide 15%, Snow Mushroom, Dist. By: @Humanrace 2022 Beverly Hills, CA 90210, USA, NDC 82779-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2624-2023·2023-09-27
FDA Recalls ALKP Chemistry Analyzer Slides for Potential Diagnostic Errors
Ortho-Clinical Diagnostics is recalling VITROS XT Chemistry ALKP Slides worldwide because high alkaline phosphatase samples may cause the analyzer to report falsely low results, potentially missing or delaying liver disease diagnoses.
Product
VITROS XT Chemistry Products ALKP Slides
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2598-2023·2023-09-27
Stryker ACM Advanced Cement Mixing System Nozzle May Disassemble
Stryker is recalling the ACM bone cement mixing system because the break-away femoral nozzle may disassemble or break off during surgery, potentially causing loss of device function and components to fall into the surgical site.
Product
Stryker ACM (Advanced Cement Mixing) System: ACM Kit w/ Femoral Breakaway Nozzle-Allows the user to mix bone cement witha constant high vacuum through the process Catalog Number: 0306-563-000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2625-2023·2023-09-27
Philips Tempus Pro Patient Monitor Software Error Impairs Critical Monitoring
Certain Philips Tempus Pro Patient Monitors may display an error message when laryngoscopes are disconnected, requiring a 60-100 second restart that prevents vital sign monitoring and airway visualization during intubation. This may lead to treatment delays or hypoxia.
Product
Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, and 00-1007, when Used With Tempus Pro Video Laryngoscope, REF 01-2044
Category
Medical Device
Distribution
42 states
HighFDA (Devices)·Z-2594-2023·2023-09-27
SofTech Wheelchair Cushions Recalled for Defective Battery Overheating Risk
Aquila Corporation is recalling 134 SofTech Pressure-Sensing Wheelchair Cushions with defective battery packs that can overheat, risking property damage and a possible injury. The affected units have been distributed nationwide in the US and internationally to Canada, Sweden, Romania, Australia, and the UK.
Product
SofTech Pressure-Sensing Wheelchair Cushions
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1151-2023·2023-09-27
FDA Recalls TRP Natural Eyes Eye Drops Due to Sterility Assurance Issue
The FDA is recalling TRP Natural Eyes Aging Eye Relief eye drops due to lack of assurance of sterility. The affected lot DB001 (expiration 06/24) was distributed to accounts in Rhode Island and Colorado.
Product
TRP Natural Eyes, Aging Eye Relief, Sterile Eye Drops, Homeopathic 0.33 FL OZ (10 mL), Manufactured in Jordan, exclusively for TRP Company, Inc., 1575 Delucchi Lane, Reno, NV 89502 NDC: 17312-027-15.
Category
Drug
Distribution
2 states
HighFDA (Drugs)·D-1154-2023·2023-09-27
TRP Natural Eyes sterile eye drops recalled for lack of sterility assurance
TRP Natural Eyes Blur Relief eye drops are being recalled due to lack of assurance of sterility. The product was distributed to accounts in Rhode Island and Colorado.
Product
TRP Natural Eyes, Blur Relief, Sterile Eye Drops, Homeopathic 0.5 FL OZ (15 mL), Manufactured in Jordan, exclusively for TRP Company, Inc., 1575 Delucchi Lane, Reno, NV 89502, NDC: 17312-002-11.
Category
Drug
Distribution
2 states
HighFDA (Drugs)·D-1160-2023·2023-09-27
FDA Recalls Eye Ointment Product Due to Sterility Assurance Failure
The FDA is recalling Major LubriFresh PM eye ointment due to lack of assurance of sterility. Approximately 282,564 units were distributed to accounts in Rhode Island and Colorado.
Product
MAJOR LubriFresh P.M. Nighttime Ointment, Lubricant Eye Ointment, Sterile, 0.125 OZ (3.5g), Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268, Made in Jordan, NDC: 0904-6488-38.
Category
Drug
Distribution
2 states
HighFDA (Drugs)·D-1176-2023·2023-09-27
Sunscreen Recall: Humanrace Ozone Body Protection Cream Lacks Declared SPF
Humanrace Suncare Ozone Body Protection Cream SPF 30 does not contain the sun protection factor declared on the label. Approximately 2,942 units have been recalled.
Product
Humanrace Suncare, Ozone Body Protection Cream, Broad Spectrum Sunscreen SPF 30, packaged as a 148mL (5 fl oz.) bottle, PA ++++, 100% mineral, Active Ingredient: Zinc oxide 15%, Snow Mushroom, Squalene, Aloe, Dist. By: @Humanrace 2022 Beverly Hills, CA 90210, USA, NDC 82779-002
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2592-2023·2023-09-27
Sentec Membrane Changer components recalled for manufacturing defect
SenTec AG recalls Membrane Changer components for the Sentec Digital Monitoring System due to a potential manufacturing defect that could affect measurement accuracy.
Product
Membrane Changer Single-Use, REF MC, each package contains 3 changers; Membrane Changer Reloadable, REF MC-R, each package contains 3 changers; and Membrane Changer Insert, REF MC-I, each package contains 5 inserts. All are components of the Sentec Digital Monitoring System…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2590-2023·2023-09-27
Arrow ErgoPack PICC Catheters Recalled for Incorrect Product Labeling
Arrow International is recalling 190 units of Arrow ErgoPack One-Lumen PICC catheters (Lot 13F22J0617) because the product code and product name were incorrectly printed on the kit packaging. The units were distributed nationwide.
Product
Arrow ErgoPack Pressure Injectable One-Lumen PICC, REF CDC-05541-HPK1A; catheter, intravascular
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1524-2023·2023-09-27
Giant Eagle Cheese Spread Recalled Due to Inconsistent Refrigeration Labels
Giant Eagle Easy Melt cheese spread products have inconsistent refrigeration instructions on their labels. The varying label requirements may cause improper storage, creating potential food safety concerns.
Product
giant eagle Easy Melt, Pasteurized Prepared Cheese Spread. Net Wt 32 oz (2lb)907g. UPC 0 30034-06289 7. Refrigerate after Opening. Distributed by Giant Eagle, Inc., Pittsburgh, PA 15328-2809.
Category
Food
Distribution
32 states
ModerateFDA (Food)·F-1530-2023·2023-09-27
HEB Easy Melt Pasteurized Cheese Spread Recalled for Conflicting Refrigeration Labels
Great Lakes Cheese is recalling HEB Easy Melt Original Pasteurized Process Cheese Spread because refrigeration instructions vary across product labels. No illnesses have been reported.
Product
Pasteurized Process Cheese Spread packaged under the following brands and sizes: 1. HEB Easy Melt Original, Net Wt 16 oz (1 lb) 453g. UPC 0 41220-73808 3. Refrigerate after Opening. Made with Pride and Care for H-E-B, San Antonio, Texas 78204 2. HEB Easy Melt Original…
Category
Food
Distribution
32 states
ModerateFDA (Food)·F-1526-2023·2023-09-27
Refrigerated Cheese Products Recalled for Conflicting Label Instructions
Great Lakes Cheese is recalling multiple brands of refrigerated pasteurized cheese products due to conflicting refrigeration instructions on product labels. The conflicting label requirements could lead to improper storage.
Product
Pasteurized Prepared Cheese Product, packaged under the following brands and sizes: 1. Clancy's CheeseMelt, 1/2 Less Fat Than Cheddar Cheese, Net Wt 32 oz (2 lbs) 907g. Refrigerate after Opening. Dist, & Sold exclusively by: Aldi, Batavia, IL 60510 2. Dutch Farms Cheese…
Category
Food
Distribution
32 states
ModerateFDA (Food)·F-1527-2023·2023-09-27
Great Value Cheese Recall Due to Inconsistent Refrigeration Label Requirements
Great Value Melt'n Dip Easy Melt Cheese is being recalled due to inconsistent refrigeration labeling requirements that may result in improper storage. The product has a use-by date of 1/4/2024 or earlier.
Product
Great Value Melt'n Dip Easy Melt Cheese, Reduced Fat Pasteurized Prepared Cheese Product, Net Wt 32 oz (2 lbs) 907g. UPC 0 78742-01517 0. Refrigerate after Opening. Distributed By: Walmart Inc., Bentonville, AR 72716
Category
Food
Distribution
32 states
ModerateFDA (Food)·F-1525-2023·2023-09-27
Pasteurized Process Cheese Spread Recalled for Conflicting Refrigeration Labels
Great Lakes Cheese and related brands recalled 7.2 million pounds of pasteurized cheese spread due to conflicting refrigeration instructions on labels that may prevent proper storage.
Product
Pasteurized Process Cheese Spread packaged under the following brands and sizes: 1. Great Lakes Cheese Easy Cheesy, Net Wt 32 oz (2lb)907g. UPC 0 36514-19245 0. Refrigerate After Purchase. Distributed by Great Lakes Cheese Co., Inc. Hiram, OH 44234 2. HEB Easy Melt Queso…
Category
Food
Distribution
32 states
ModerateFDA (Food)·F-1532-2023·2023-09-27
Refrigerated Cheese Products Recalled for Unclear Refrigeration Label Requirements
Great Lakes Cheese, Inc. is recalling refrigerated cheese products because product labels have varying refrigeration requirements that could lead to improper storage. Approximately 7.2 million lbs of products sold under Clancy's and Hill Country Fare brands are affected.
Product
Pasteurized Prepared Cheese Product, Queso Blanco, Half the Fat of Cheddar Cheese packaged under the following brands and sizes: 1. Clancy's CheeseMelt, Net Wt 32 oz (2 lbs) 907g. Refrigerate after Opening. Dist, & Sold exclusively by: Aldi, Batavia, IL 60510 2. Hill…
Category
Food
Distribution
32 states
ModerateFDA (Food)·F-1531-2023·2023-09-27
Pasteurized Cheese Product Recalled for Inconsistent Refrigeration Instructions on Labels
Great Lakes Cheese, Inc. is recalling Hill Country Fare Melt'n Cheese because product labels contain inconsistent refrigeration requirements, which may result in improper storage by consumers.
Product
Hill Country Fare Melt'n Cheese, Pasteurized Prepared Cheese Product, Net Wt 32 oz (2 lbs) 907g. UPC 0 41220-77273 5. Refrigerate after Opening. Distributed By: H-E-B, San Antonio, TX 78204
Category
Food
Distribution
32 states
ModerateFDA (Food)·F-1533-2023·2023-09-27
HEB Easy Melt Salsa Queso Recalled Due to Conflicting Refrigeration Labels
HEB Easy Melt Salsa Queso is recalled for conflicting refrigeration labels that may cause improper storage. Over 7.2 million pounds were distributed across 32 states.
Product
HEB Easy Melt Salsa Queso, with Tomatoes, Jalapeno Peppers & Onions, Net Wt 32 oz (2 lbs) 907g. UPC 0 41220-33063 8. Refrigerate after Opening. Made with Pride and Care for H-E-B, San Antonio, Texas 78204
Category
Food
Distribution
32 states
ModerateFDA (Devices)·Z-2613-2023·2023-09-27
Prucka 3 Amplifier Power Supply May Fail and Cause Device Inoperability
GE Medical Systems is recalling Prucka 3 Amplifiers and related field replaceable units used in CardioLab and ComboLab systems. A power supply diode may overheat and fail, causing the amplifier to stop working.
Product
Prucka 3 Amplifiers, Model P1801PA, and Field Replaceable Units (FRUs), Model 5875569, used with CardioLab AltiX and ComboLab AltiX.
Category
Medical Device
Distribution
17 states
ModerateFDA (Food)·F-1528-2023·2023-09-27
Refrigerated Pasteurized Cheese Products Recalled Due to Labeling Inconsistency
Great Value and SE Grocers refrigerated cheese products are being recalled because labels contain inconsistent refrigeration requirements, which may result in improper storage by consumers.
Product
Pasteurized Prepared Cheese Product packaged under the following brands and sizes: 1. Great Value Original Melt'n Dip Easy Melt Cheese, Net Wt 16 oz (1 lb) 453g. UPC 0 78742-01512 5. Refrigerate after Opening. Distributed By: Walmart Inc., Bentonville, AR 72716 2.…
Category
Food
Distribution
32 states
ModerateFDA (Drugs)·D-1168-2023·2023-09-27
ChloraPrep One-Step Topical Applicators Recalled for Unsupported Shelf-Life Claims
BD ChloraPrep One-Step topical applicators are recalled because the 36-month shelf life is not supported by stability data; the product may develop fungal contamination beyond 12 months.
Product
CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1529-2023·2023-09-27
Harris Teeter Cheesy Melt recalled for labeling refrigeration requirements
Harris Teeter Cheesy Melt pasteurized cheese product is recalled because labeling variations may prevent proper refrigeration. Approximately 7.2 million pounds are affected across 31 states with use-by dates of March 8, 2024 and earlier.
Product
Harris Tetter Cheesy Melt, Pasteurized Prepared Cheese Product, Net Wt 32 oz (2 lbs) 907g. UPC 0 72036-70682 9. After Opening, Refrigerate Up to 8 weeks. Do Not Freeze. Proudly Distributed By: Harris Teeter, LLC, Matthews, NC 28105
Category
Food
Distribution
32 states