Colorado recalls
3,557 federal recalls affecting Colorado in the last 12 months - 195 Colorado-specific plus 3,362 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-01-14FDA-DeviceAVID MedicalClass INationwideStop using Halyard ORGAN RECOVERY OR PACK
Halyard ORGAN RECOVERY OR PACK (Kit Code LLOG1000-15) devices have been found to be unsuitable for organ transplant use. The FDA has issued a Class I recall affecting 132 units distributed in Florida, Georgia, and Puerto Rico. No injuries have been reported.
- 2026-01-14FDA-DeviceSiemensClass IINationwideContact Siemens about your LUMINOS X-ray system
Siemens LUMINOS Lotus Max and Luminos dRF Max X-ray systems with software version VF11 may show incorrect collimation (beam positioning) when quickly switching between organ programs. This affects only systems with a bucky wall stand for mobile detectors and no ceiling stand.
- 2026-01-14FDA-DeviceVision RTClass IINationwideCheck AlignRT InBore documentation for laser details
Vision RT identified that instructions for the AlignRT InBore radiation therapy system omitted required information about its six Class 1 lasers and their specifications. The missing details are required by federal laser safety regulations. No injuries have been reported.
- 2026-01-14FDA-FoodMAYEJClass IINationwideStop using MAYEJ Italian Parsley
MAYEJ Italian Parsley packaged in 24lb boxes has been recalled due to potential contamination with Cyclospora cayetanensis, a parasite that can cause foodborne illness. About 1,288 boxes were distributed nationwide. No illnesses have been reported so far.
- 2026-01-14FDA-FoodDirect Source SeafoodClass IIDon't eat Market 32 frozen raw shrimp
Market 32 brand frozen raw shrimp (26/30 count, 16 oz packages) from Indonesia may be contaminated with Cesium-137, a radioactive substance. The affected shrimp were distributed to stores in Connecticut, Massachusetts, New Hampshire, New York, Pennsylvania, and Vermont with best-by dates between April 22 and April 27, 2027.
- 2026-01-14FDA-FoodDirect Source SeafoodClass IIwaterfront BISTRO brand Frozen Raw Shrimp EZ PEEL SHELL & TAIL ON Colossal 8-12 Count per Lb. Net wt. 32oz (2LB). Product is packaged in white flexible plastic pouch with multicolored labeling. UPC is 0 21130 13224 9. Product of Indonesia. DISTRIBUTED BY LUCERNE FOODS, INC. P.O. BOX 99 PLEASANTON, CA 94566.
Shrimp may be contaminated with Cesium-137 (Cs-137).
- 2026-01-14FDA-FoodZiyadClass IINationwideStop eating Baraka Gourmet Pastry Kunafe
Ziyad Brothers Importing is recalling Baraka Gourmet Pastry Kunafe (6.7 oz) because it may contain partially hydrogenated oils that are not listed on the label. Partially hydrogenated oils contain trans fats, which are not permitted in food sold in the United States. No injuries have been reported.
- 2026-01-14FDA-FoodZiyadClass IINationwideCheck your Baraka puff pastry for recall
Ziyad Brothers Importing is recalling Baraka French Style Puff Pastry in 1lb and 1.5lb sizes because they may contain partially hydrogenated oils that are not listed on the label. Partially hydrogenated oils are banned in most foods in the United States. No injuries have been reported.
- 2026-01-14FDA-FoodMcCainClass IIStop using Sysco Imperial Potato Tater Barrel
McCain Foods USA Inc is recalling Sysco Imperial Potato Tater Barrel frozen potatoes because some packages may contain hard plastic fragments. The affected product was distributed across 26 states in specific batch codes produced in October and November 2025. No injuries have been reported.
- 2026-01-14FDA-FoodMcCainClass IIStop using Ore-Ida Tater Tots item OIF00215A
Ore-Ida Tater Tots shaped potatoes (item OIF00215A, 30 lb cases) may contain clear hard plastic fragments. The affected product was produced between October 9–14, 2027, and distributed to foodservice locations across 27 states. No injuries have been reported.
- 2026-01-14FDA-FoodAmbriolaClass IStop using Locatelli Grated Pecorino Romano
Locatelli Grated Pecorino Romano cheese in 8 oz plastic cups has been recalled because it tested positive for Listeria Monocytogenes, a bacteria that can cause serious illness. The affected product was distributed across multiple states in the U.S.
- 2026-01-14FDA-FoodAmbriolaClass IStop using Ambriola Piccante Pecorino Romano cheese
Ambriola Co., Inc. is recalling grated Pecorino Romano cheese in 5 and 10-pound bags because the product tested positive for Listeria monocytogenes, a bacteria that can cause serious illness. The recalled cheese was distributed across multiple states.
- 2026-01-14FDA-FoodAmbriolaClass IDiscard Boar's Head Pecorino Romano Grated cheese
Boar's Head Pecorino Romano Grated cheese in 5-pound bags tested positive for Listeria monocytogenes, a bacterium that can cause serious illness. The affected product was distributed across multiple states. No illnesses have been reported so far.
- 2026-01-14FDA-FoodAmbriolaClass IStop using Sam's Pecorino Romano grated cheese
Sam's Pecorino Romano grated cheese in 1.5 lb plastic bags tested positive for Listeria Monocytogenes, a bacteria that can cause serious illness. The affected product was distributed across multiple states. No illnesses have been reported to date.
- 2026-01-14FDA-FoodAmbriolaClass IDiscard Boar's Head Pecorino Romano cheese
Boar's Head grated Pecorino Romano cheese in 6 oz cups tested positive for Listeria monocytogenes, a bacteria that can cause serious illness. The affected product has lot number 1000572486 and was distributed across multiple states.
- 2026-01-14FDA-FoodAmbriolaClass IStop using Pinna Grated Pecorino Romano
Pinna Grated Pecorino Romano cheese in 10-pound bags tested positive for Listeria Monocytogenes, a bacteria that can cause serious illness. The affected product was distributed across multiple states. No illnesses have been reported so far.
- 2026-01-14FDA-FoodAmbriolaClass IStop using Locatelli Grated Pecorino Romano
Locatelli Grated Pecorino Romano cheese in 5 and 10-pound bags tested positive for Listeria monocytogenes, a bacterium that can cause serious illness. The affected product was distributed across 20 states. No illnesses have been reported so far.
- 2026-01-14FDA-FoodAmbriolaClass IDo not eat Locatelli Grated Pecorino Romano
Locatelli Grated Pecorino Romano cheese in 4 oz and 8 oz plastic cups tested positive for Listeria Monocytogenes, a bacteria that can cause serious illness. The affected product was distributed across multiple U.S. states.
- 2026-01-14FDA-FoodSam Dry Fruits and NutsClass INationwideDon't eat Sam Dry Fruits & Nuts pistachios
Sam Dry Fruits & Nuts Enterprises is recalling whole pistachio meats (Lot #PK00459, 30-lb bags, pack date August 2025) because they may be contaminated with Salmonella, a bacteria that can cause serious illness. This is a Class I recall, the most serious type. No illnesses have been reported so far.
- 2026-01-14FDA-DrugAvKAREClass IINationwideStop using AvKARE Rosuvastatin 10 mg tablets
AvKARE is recalling Rosuvastatin 10 mg tablets (Lot #49124, expiring 12/31/2026) because they don't dissolve properly in the body. This means the medication may not work as intended. No injuries have been reported so far.
- 2026-01-14FDA-DrugMedinaturaClass INationwideStop using ClearLife Allergy Nasal Spray
ClearLife Allergy Nasal Spray Extra Strength has been found to contain yeast, mold, and a bacterium called Achromobacter. The contamination affects all batches still within their expiration date sold nationwide. No injuries have been reported so far.
- 2026-01-14FDA-DrugMedinaturaClass INationwideStop using MediNatura ReBoost Nasal Spray
MediNatura ReBoost Nasal Spray has been found to contain yeast, mold, and a bacterium called Achromobacter. These contaminants should not be in a nasal spray, which is meant to be sterile. The contamination affects all lots currently in use.
- 2026-01-14FDA-DrugSpecGxClass IINationwideCheck your SpecGx pain medication bottle
SpecGx LLC is recalling one lot of oxycodone and acetaminophen tablets (7.5 mg/325 mg) because some tablets may be missing the imprint (identifying mark). This makes it difficult to verify you have the correct medication. No injuries have been reported.
- 2026-01-14FDA-DrugSpecGxClass IINationwideCheck your SpecGx oxycodone tablets
SpecGx LLC is recalling certain bottles of oxycodone and acetaminophen 10mg/325mg tablets because some tablets may be missing the imprint (marking). This could make it difficult to identify the medication. No injuries have been reported.
- 2026-01-14FDA-DrugImprimisClass IINationwideStop using Imprimis Tri-Moxi eye injections
Imprimis NJOF recalled Tri-Moxi+ eye injections because some batches contain glass-like particles. The affected batches (25JAN033A and 25JAN033B) expire in February 2026. No injuries have been reported.
- 2026-01-14FDA-DrugImprimisClass IINationwideStop using Imprimis NJOF eye injection
Imprimis NJOF's dexamethasone-moxifloxacin-ketorolac eye injection contains glass-like particles that could contaminate the injection. This medication is used during eye surgery. The affected lots are 25APR001A and 25APR001B, expiring 04/03/2026.
- 2026-01-14FDA-DrugImprimisClass IINationwideStop using Imprimis eye injection immediately
Imprimis NJOF, LLC is recalling specific lots of Dexamethasone Moxifloxacin intraocular injection due to the presence of glass-like particles in the medication. This injection is used during eye surgery. Two affected lots have been identified and distributed nationwide.
- 2026-01-14FDA-DrugAlembic PharmaceuticalsClass IIINationwideStop using Alembic Fesoterodine Fumarate tablets
Alembic Pharmaceuticals is recalling one lot of Fesoterodine Fumarate 8 mg extended-release tablets because testing found levels of a chemical impurity (diester impurity) that exceed safety limits. The affected lot is 2405003360, which expires January 31, 2026.
- 2026-01-08CPSCJoyful JourneysNationwideStop using Joyful Journeys baby loungers immediately
Joyful Journeys baby loungers have sides that are too low and openings that are too wide, creating risks that infants could fall out or become trapped. The loungers also lack a stand, making them unsafe on elevated surfaces. These design flaws violate federal safety standards for infant sleep products.
- 2026-01-08CPSCPNW ComponentsNationwideStop using PNW Components Loam Pedal Gen 2
The axle on PNW Components Loam Pedal Gen 2 mountain bike pedals can crack and cause the pedal to detach from your bike while riding, creating a fall risk. The company has received four reports of this problem, though no injuries have been reported yet.
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