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. 2,489 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,489 in last 12 months

Showing 3342133440 of 51,434 recalls

DrugAugust 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...

The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...

The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2016· Sandoz Inc

Recalled Item: Phenylephrine HCI Injection Recalled by Sandoz Inc Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...

The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...

The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...

The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2016· Amerisource Health Services

Recalled Item: Dextroamphetamine Saccharate Recalled by Amerisource Health Services Due to...

The Issue: Unit Dose Mispackaging; blister cavities may contain more than one tablet...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 23, 2016· Integra LifeSciences Corp.

Recalled Item: Integra Ventricular Catheter Accessory Kit Recalled by Integra LifeSciences...

The Issue: During final sampling inspection, one of the lots was discovered with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2016· Integra LifeSciences Corp.

Recalled Item: Integra Straight Ventricular Catheter F8 Recalled by Integra LifeSciences...

The Issue: During final sampling inspection, one of the lots was discovered with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2016· Integra LifeSciences Corp.

Recalled Item: Integral Lumbar Drainage Set Recalled by Integra LifeSciences Corp. Due to...

The Issue: During final sampling inspection, one of the lots was discovered with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2016· Integra LifeSciences Corp.

Recalled Item: CUSA Dissectron Fingertip Laparoscopic Cannula Recalled by Integra...

The Issue: During final sampling inspection, one of the lots was discovered with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2016· Integra LifeSciences Corp.

Recalled Item: Integra Drainage Accessory Kits Recalled by Integra LifeSciences Corp. Due...

The Issue: During final sampling inspection, one of the lots was discovered with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2016· Integra LifeSciences Corp.

Recalled Item: Integra Lumbar Drainage Set Recalled by Integra LifeSciences Corp. Due to...

The Issue: During final sampling inspection, one of the lots was discovered with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2016· Hologic, Inc

Recalled Item: Sertera Biopsy Device Recalled by Hologic, Inc Due to Incorrect label on the...

The Issue: Incorrect label on the Sertera Biopsy Kit

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2016· EKOS Corporation

Recalled Item: The EKOS cart has the catalog number 700-60101. The EKOS Recalled by EKOS...

The Issue: Casters on the EKOS carts may be missing washers which can cause premature...

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

Class II — Potential Health HazardOngoing
DrugAugust 22, 2016· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2016· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2016· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Transdermal Patch Recalled by...

The Issue: Defective Delivery System: Out of Specification (OOS) results for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 19, 2016· Impax Laboratories, Inc.

Recalled Item: Lamotrigine Orally Disintegrating Tablets (ODT) Recalled by Impax...

The Issue: Labeling; Label Mixup; box labeled to contain 200 mg blister packs but...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 19, 2016· Unichem Pharmaceuticals Usa Inc

Recalled Item: Lamotrigine Tablets Recalled by Unichem Pharmaceuticals Usa Inc Due to...

The Issue: Tablets/Capsules Imprinted With Wrong ID: incorrect imprint debossed on the...

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

Class III — Low RiskOngoing
Refund