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 2094120960 of 51,434 recalls

Medical DeviceOctober 3, 2019· Ethicon Endo-Surgery Inc

Recalled Item: ECHELON FLEX ENDOPATH 60mm Stapler - 340mm shaft Recalled by Ethicon...

The Issue: The staplers may contain an out of specification anvil component within the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 3, 2019· Philips North America, LLC

Recalled Item: HeartStart XL+ Defibrillator/Monitor Recalled by Philips North America, LLC...

The Issue: Device may fail to turn on or unexpectedly attempt to restart, rendering it...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2019· Ethicon Endo-Surgery Inc

Recalled Item: ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 340mm shaft Recalled by...

The Issue: The staplers may contain an out of specification anvil component within the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 3, 2019· Ethicon Endo-Surgery Inc

Recalled Item: ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 440mm shaft Recalled by...

The Issue: The staplers may contain an out of specification anvil component within the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 3, 2019· Ethicon Endo-Surgery Inc

Recalled Item: ECHELON FLEX Powered Plus ENDOPATH 60mm Stapler - 280mm shaft Recalled by...

The Issue: The staplers may contain an out of specification anvil component within the...

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

Class I — Serious Health HazardOngoing
FoodOctober 3, 2019· Arcadia Trading Inc.

Recalled Item: Dried Mushroom NET WT: 8oz (227g) Ingredients: Mushroom Distributed By:...

The Issue: Product contains undeclared sulfites.

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 2, 2019· Exactech, Inc.

Recalled Item: 2.4mm x 2.5 Fluted Pin Pouch Recalled by Exactech, Inc. Due to Potential for...

The Issue: Potential for the 2.4mm x 2.5 Fluted Pin Pouch to contain a single pin...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2019· Pega Medical Inc.

Recalled Item: SCFE (slipped capital femoral epiphysis) Knobs for Driver Recalled by Pega...

The Issue: There is a potential for the screws to have become loosened during...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2019· Zeiss, Carl Inc

Recalled Item: Component for Laser Scanning Microscopes (LSM 700 Recalled by Zeiss, Carl...

The Issue: When the user tilts the transmitted light arm of the microscope to the end...

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

Class II — Potential Health HazardOngoing
DrugOctober 2, 2019· Pfizer Inc.

Recalled Item: 10% LMD in 5% Dextrose Injection Dextran 40 in Dextrose Injection Recalled...

The Issue: Lack of Assurance of Sterility: Bag has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 1, 2019· Sato Pharmaceutical Inc.

Recalled Item: Motion Sickness (meclizine hydrochloride) 25 mg tablets Recalled by Sato...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugOctober 1, 2019· Sato Pharmaceutical Inc.

Recalled Item: Sankaijo BOTANICAL LAXATIVE (docusate sodium 8.33 mg and sennosides 1.36...

The Issue: Subpotent Drug: Formulated amount of sennosides component is less than...

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

Class III — Low RiskOngoing
Refund
DrugOctober 1, 2019· New Vitalis Pharmacy LLC dba New Vitalis Pharmacy

Recalled Item: Testosterone Cypionate 180 mg/mL/Testosterone Propionate 20mg/mL Oil...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 1, 2019· Sato Pharmaceutical Inc.

Recalled Item: Zentrip (meclizine Hydrochloride) Recalled by Sato Pharmaceutical Inc. Due...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugOctober 1, 2019· Sato Pharmaceutical Inc.

Recalled Item: Motion Sickness Strips (meclizine hydrochloride) 25 mg strips Recalled by...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugOctober 1, 2019· Sato Pharmaceutical Inc.

Recalled Item: WAL-DRAM 2 (meclizine Hydrochloride) 25 mg tablets Recalled by Sato...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 1, 2019· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Rosebud Vital Signs Monitor with NIBP valve assembly board Recalled by...

The Issue: NIBP valve assembly board subject to this recall includes enhancements that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Accutorr 7 Vital Signs Monitor with NIBP valve assembly board Recalled by...

The Issue: NIBP valve assembly board subject to this recall includes enhancements that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: BardPort M.R.I. Implantable Port with Attachale 9.6 F Open-Ended...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2019· Bard Peripheral Vascular Inc

Recalled Item: BardPort Titanium Implantable Port with Attachable 9.6 F Open-Ended...

The Issue: Firm has identified that the product may be at risk of incorrectly...

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

Class II — Potential Health HazardOngoing