Product Recalls in Colorado

Product recalls affecting Colorado — including food, drugs, consumer products, medical devices, and vehicles distributed to Colorado. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,551 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,551 in last 12 months

Showing 2028120300 of 51,434 recalls

DrugDecember 10, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Memantine Hydrochloride Extended-release Capsules Recalled by Lupin...

The Issue: Failed Dissolution Specifications: High out of specification result observed...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 10, 2019· bioMerieux, Inc.

Recalled Item: VIDAS Varicella Zoster IgG (VZG) antibody IVD Recalled by bioMerieux, Inc....

The Issue: Two batches of VIDAS Varicella-Zoster IgG (VZG ) may yield an invalid...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2019· Abbott Medical

Recalled Item: Fast-Cath Trio HEMOSTASIS INTRODUCER Recalled by Abbott Medical Due to...

The Issue: Fast-Cath Trio Hemostasis Introducer devices contained 12F sized dilators...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2019· Abbott Medical

Recalled Item: Fast-Cath Hemostasis Introducer Recalled by Abbott Medical Due to Three lots...

The Issue: Three lots of Fast-Cath Hemostasis Introducer devices contained 8F sized...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 6, 2019· Lannett Company, Inc.

Recalled Item: Levetiracetam Oral Solution 100mg/mL Recalled by Lannett Company, Inc. Due...

The Issue: Microbial Contamination of Non-sterile Products: Out-of-specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
FoodDecember 6, 2019· Ferris Coffee and Nut Company, Inc.

Recalled Item: R.H. Macys & Co. Cinnamon Roasted Almonds Recalled by Ferris Coffee and Nut...

The Issue: Incorrect product label on back panel

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodDecember 6, 2019· Ferris Coffee and Nut Company, Inc.

Recalled Item: R.H. Macys & Co. Roasted Salted Cherries Berries and Nuts with Dark...

The Issue: Incorrect product label on back panel, undeclared cashew, pecan, milk and soy

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 6, 2019· Karl Storz Endoscopy

Recalled Item: Karl Storz SE & Co. KG Recalled by Karl Storz Endoscopy Due to The firm has...

The Issue: The firm has become aware that there is a potential that the glass cover at...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2019· Medtronic Navigation, Inc.

Recalled Item: Mazor X Surgical System Positioner Type II Recalled by Medtronic Navigation,...

The Issue: There is a potential for the surgical system to detach from the operational...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2019· Stryker GmbH

Recalled Item: Stryker T2 Alpha Delta Strike Plate IMN Instruments - part Recalled by...

The Issue: Instrument can break at the level of the thread when being exposed to high...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 4, 2019· American Health Packaging

Recalled Item: Raloxifene Hydrochloride Tablets Recalled by American Health Packaging Due...

The Issue: Failed Dissolution Specifications: Low out of specification results obtained...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodDecember 4, 2019· CHICKEN OF THE SEA

Recalled Item: Chicken of the Sea Sardines in Water Recalled by CHICKEN OF THE SEA Due to...

The Issue: It was discovered that one batch of sardines were incorrectly labeled -...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodDecember 4, 2019· Werner Gourmet Meat Snacks, Inc.

Recalled Item: Jolly Rancher product is hard candies Recalled by Werner Gourmet Meat...

The Issue: Jolly Rancher product is recalled due to undeclared soy lecithin.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodDecember 3, 2019· Mrs. Condies Salad Company, Incorporated

Recalled Item: Mrs. Condies Salad Company's Honey Bear Small Party Platter containing...

The Issue: Ranch Dressing dip contains undeclared milk as an ingredient.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 3, 2019· GE Healthcare, LLC

Recalled Item: Lunar iDXA Advance (iDXA with enCORE v16) bone densitometer Recalled by GE...

The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2019· GE Healthcare, LLC

Recalled Item: Lunar iDXA bone densitometer Recalled by GE Healthcare, LLC Due to An issue...

The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2019· GE Healthcare, LLC

Recalled Item: Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v18) bone densitometer...

The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2019· GE Healthcare, LLC

Recalled Item: Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v17) bone densitometer...

The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2019· Johnson & Johnson Surgical Vision Inc

Recalled Item: Healon GV PRO 0.85 mL Recalled by Johnson & Johnson Surgical Vision Inc Due...

The Issue: Ophthalmic viscosurgical device may be difficult to remove from the eye,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 2, 2019· AuroMedics Pharma LLC

Recalled Item: Moxifloxacin Ophthalmic Solution USP Recalled by AuroMedics Pharma LLC Due...

The Issue: Discoloration: Market complaints of discoloration in Moxifloxacin Ophthalmic...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund