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 2078120800 of 51,434 recalls

Medical DeviceOctober 21, 2019· Haemonetics Corporation

Recalled Item: Japan CS Elite FASTPACK DISP. SET - 125ML - Product Recalled by Haemonetics...

The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Haemonetics Corporation

Recalled Item: JAPAN DISP SET Recalled by Haemonetics Corporation Due to Potential to...

The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Haemonetics Corporation

Recalled Item: Cell Saver¿5/5+ Bowl Kit (225 ml) Autotransfusion Device - Product Recalled...

The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Haemonetics Corporation

Recalled Item: CS Elite Fastpack Recalled by Haemonetics Corporation Due to Potential to...

The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...

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

Class II — Potential Health HazardOngoing
DrugOctober 21, 2019· Nephron Pharmaceuticals Corporation dba Nephron Sterile Compounding Center

Recalled Item: PF-Succinylcholine Chloride Injection Recalled by Nephron Pharmaceuticals...

The Issue: Incorrect 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
Medical DeviceOctober 21, 2019· Beckman Coulter Inc.

Recalled Item: DxM 1040 MicroScan WalkAway Instrument Recalled by Beckman Coulter Inc. Due...

The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Beckman Coulter Inc.

Recalled Item: DxM 1096 MicroScan WalkAway Instrument Recalled by Beckman Coulter Inc. Due...

The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-40 plus Instrument Recalled by Beckman Coulter Inc. Due...

The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-96 plus Instrument Recalled by Beckman Coulter Inc. Due...

The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-96 plus Reconditioned Instrument Recalled by Beckman...

The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-40 plus Reconditioned Instrument Recalled by Beckman...

The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...

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

Class II — Potential Health HazardOngoing
DrugOctober 18, 2019· Mylan Pharmaceuticals Inc.

Recalled Item: Prasugrel Tablets 5 mg Recalled by Mylan Pharmaceuticals Inc. Due to Failed...

The Issue: Failed Dissolution Specification: Low out of specification dissolution results.

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 18, 2019· Cold Locker Processing LLC

Recalled Item: Kroger Wild Caught Sockeye Salmon Boneless Recalled by Cold Locker...

The Issue: Kroger Wild Caught Sockeye Salmon, Frozen, is recalled due to a potential...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 18, 2019· Brasseler USA I Lp

Recalled Item: BRASSELER KM166-310-35 Twist Drill Quick Connect Diameter 3.5 mm Recalled by...

The Issue: One lot of 3.5 mm twist drills were incorrectly laser etched as 2.5 mm the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2019· Capso Vision, Inc.

Recalled Item: CapsoCAM Plus Recalled by Capso Vision, Inc. Due to Capsule Endoscopy...

The Issue: Capsule Endoscopy System: a defect present in the capsule window may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2019· Tornier, Inc

Recalled Item: Aequalis Ascend Flex Humeral Stem: Part Number UDI DWF601A 3700386944475...

The Issue: During shipping, it is possible for the Aequalis Ascend Flex humeral stem to...

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

Class II — Potential Health HazardOngoing
DrugOctober 17, 2019· AVKARE Inc.

Recalled Item: AVKARE Ranitidine Hydrochloride Capsules 300 mg 500 Capsules Rx Only...

The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 17, 2019· Sandoz Inc

Recalled Item: Gatifloxacin Ophthalmic Solution 0.5% Recalled by Sandoz Inc Due to...

The Issue: Labeling: Incorrect or missing package insert.

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

Class III — Low RiskOngoing
Refund
DrugOctober 17, 2019· Sandoz Inc

Recalled Item: Neomycin and Polymyxin B Sulfates and Dexamethasone Ophthalmic Suspension...

The Issue: Labeling: Incorrect or missing package insert.

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

Class III — Low RiskOngoing
Refund
DrugOctober 17, 2019· AVKARE Inc.

Recalled Item: AVKARE Ranitidine Hydrochloride Capsules 150 mg 500 Capsules Rx Only...

The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API

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

Class II — Potential Health HazardOngoing
Refund