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. 2,509 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,509 in last 12 months

Showing 2846128480 of 51,434 recalls

DrugSeptember 26, 2017· Pharmedium Services, LLC

Recalled Item: morphine Sulfate in 0.9% Sodium Chloride Injection 2 mL Total Recalled by...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date

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

Class III — Low RiskOngoing
Refund
DrugSeptember 26, 2017· Pharmedium Services, LLC

Recalled Item: Phenylephrine HCL 100 mcg per mL (1 mg/10 mL) in Recalled by Pharmedium...

The Issue: Superpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 26, 2017· The Harvard Drug Group

Recalled Item: Alprazolam Tablets Recalled by The Harvard Drug Group Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 25, 2017· Sandoz Inc

Recalled Item: Ampicillin for Injection Recalled by Sandoz Inc Due to Labeling: Missing...

The Issue: Labeling: Missing Label: customer complaint that some vials of ampicillin...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2017· Precision Dose Inc.

Recalled Item: Carbamazepine Oral Suspension USP Recalled by Precision Dose Inc. Due to...

The Issue: Subpotent Drug: low out of specification results.

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

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2017· Amneal Pharmaceuticals, Inc.

Recalled Item: Esterified Estrogens & Methyltestosterone Tablets Recalled by Amneal...

The Issue: Subpotent Drug: Out of specification assay result in Esterified Estrogen and...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2017· Amneal Pharmaceuticals, Inc.

Recalled Item: Esterified Estrogens & Methyltestosterone Tablets Recalled by Amneal...

The Issue: Subpotent Drug: Out of specification assay result in Esterified Estrogen and...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 25, 2017· Smiths Medical ASD Inc.

Recalled Item: CADD(TM) Medication Cassette Reservoir with clamp and female Luer. Nonvented...

The Issue: Smiths Medical became aware that certain Non Flow-Stop CADD(R) Medication...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2017· Smiths Medical ASD Inc.

Recalled Item: CADD(TM) Yellow Medication Cassette Reservoir with clamp and female Luer....

The Issue: Smiths Medical became aware that certain Non Flow-Stop CADD(R) Medication...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2017· Smiths Medical ASD Inc.

Recalled Item: CADD(TM) Medication Cassette Reservoir with clamp and female Luer. Recalled...

The Issue: Smiths Medical became aware that certain Non Flow-Stop CADD(R) Medication...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2017· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products DAT Performance Verifier V in vitro diagnostic...

The Issue: This product is not meeting the current storage labeling for unopened VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2017· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products DAT Performance Verifier I in vitro diagnostic...

The Issue: This product is not meeting the current storage labeling for unopened VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2017· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products DAT Performance Verifier III in vitro diagnostic...

The Issue: This product is not meeting the current storage labeling for unopened VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2017· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products DAT Performance Verifier II in vitro diagnostic...

The Issue: This product is not meeting the current storage labeling for unopened VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2017· Guangzhou Improve Medical Instruments Co., Ltd.

Recalled Item: Prevent G Safety Winged Blood Collection Set Glide - Rx Recalled by...

The Issue: Complain due to the hub needle came out when the nurse draw the blood and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2017· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products DAT Performance Verifier IV in vitro diagnostic...

The Issue: This product is not meeting the current storage labeling for unopened VITROS...

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

Class II — Potential Health HazardOngoing
FoodSeptember 22, 2017· The Kroger Co

Recalled Item: Chicken Salad Sandwich 6.8 oz plastic container Contains: Wheat Recalled by...

The Issue: The firm was notified by their manufacturer that the product is contaminated...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 22, 2017· Silver Spring Foods, Inc.

Recalled Item: waterfront Bistro Tatar Sauce Recalled by Silver Spring Foods, Inc. Due to...

The Issue: Silver Spring is recalling Waterfront Bistro Tartar Sauce because an...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 22, 2017· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Mobic (meloxicam) tablets Recalled by Boehringer Ingelheim Pharmaceuticals,...

The Issue: Labeling: Incorrect or missing package insert. One lot of Mobic Tablets is...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 21, 2017· Medline Industries Inc

Recalled Item: Medline Catheter Insertion Kit Recalled by Medline Industries Inc Due to...

The Issue: Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep...

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

Class II — Potential Health HazardOngoing
Refund