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. 945 recalls have been distributed to Colorado in the last 12 months.
Showing 46281–46300 of 51,434 recalls
Recalled Item: ANGIOGRAPHY PACK Recalled by Medline Industries, Inc. Due to Guidewire...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Fabius GS Premium Recalled by Draeger Medical, Inc. Due to During...
The Issue: During final testing of the Draeger Fabius GS Premium, Fabius OS, and Fabius...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CATH LAB CUSTOM PACK Recalled by Medline Industries, Inc. Due to Guidewire...
The Issue: Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine Hydrochloride 2% and Epinephrine 1:100 Recalled by Novocol...
The Issue: Subpotent Drug; Two lots of Lidocaine 2% with Epinephrine 1:100,000...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: Visible particulate embedded in the glass...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CARBOplatin Injection Recalled by Teva Pharmaceuticals USA, Inc. Due to Lack...
The Issue: Lack of Assurance of Sterility: The required reduction of endotoxin was not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Siemens EasyLink Informatics System V4.0/V5 Siemens Recalled by Siemens...
The Issue: May not perform as intended under certain conditions, causing the release of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Kit (6 units) Recalled by Codman & Shurtleff, Inc. Due to Drug...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Kit (1 unit) Recalled by Codman & Shurtleff, Inc. Due to Drug flow...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Application Instrument Sternal Zip Flex System intended for use...
The Issue: When using the 1st generation Zip Fix Application Instrument it is possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Pump Recalled by Codman & Shurtleff, Inc. Due to Drug...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AEQUALIS Reversed II or AEQUALIS Reversed Fracture Impactor. These products...
The Issue: Following the identification of the disassociation of an impactor tip during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cypher MIS Screw System Recalled by Ebi, Llc Due to Several complaints were...
The Issue: Several complaints were reported to exhibit screw head splay in the Cypher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Pump Recalled by Codman & Shurtleff, Inc. Due to Drug...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Kit Recalled by Codman & Shurtleff, Inc. Due to Drug flow rates...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Kit Recalled by Codman & Shurtleff, Inc. Due to Drug flow rates...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Pump Recalled by Codman & Shurtleff, Inc. Due to Drug...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Pump Recalled by Codman & Shurtleff, Inc. Due to Drug...
The Issue: Drug flow rates exceeding programmed flow rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Dressing Change Kit Recalled by Churchill Medical Systems, Inc. Due...
The Issue: Microbore tubing disconnecting from male luers on the extension sets.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clinical Chemistry Phosphorus Reagent The Phosphorus assay is used for...
The Issue: Reagent lots 64736UN12, 03991UN13, 51611UN13, 74805UN12, and 03992UN13 have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.