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. 1,063 recalls have been distributed to Colorado in the last 12 months.
Showing 21701–21720 of 51,434 recalls
Recalled Item: Dynex DSX Software-IVD ELISA Assays effected as follows: DSX Assay Recalled...
The Issue: Assay files used on the open Dynex DSX Instrument to process IVD ELISA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm FDR Go Plus mobile X-ray system Recalled by Fujifilm Medical...
The Issue: The graphics driver of the FDR Go PLUS might cause the appearance of a Blue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NobelActive Internal NP 3.5x15mm Endosseus dental implant Recalled by Nobel...
The Issue: The top label for dental implant may incorrectly indicate the implant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Corporation Due to Complaints have been received...
The Issue: Complaints have been received regarding difficulty in removing the driver...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Corporation Due to Complaints have been received...
The Issue: Complaints have been received regarding difficulty in removing the driver...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-TEMP LT System Recalled by Cincinnati Sub-Zero Products LLC, a...
The Issue: Updated Manual-Warnigs have been added stating that exceeding 40'C for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips 5-Lead Set Recalled by Philips North America, LLC Due to The...
The Issue: The thickness of the connector to the trunk cable on affected limb lead sets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lisinopril and Hydrochlorothiazide Tablets USP Recalled by Lupin...
The Issue: Presence of Foreign Tablets/Capsules: Product complaint received of one...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MONSEL'S (Ferric Subsulfate) Solution Recalled by Dercher Enterprises, Inc.,...
The Issue: Microbial Contamination of Non-Sterile Products and Superpotent Drug: FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corporation...
The Issue: Lack of Assurance of Sterility: Bags have potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylergonovine Maleate USP 0.2 mg Tablets a) 12 count (NDC Recalled by...
The Issue: Presence of Foreign Tablet/Capsule; one Promethazine tablet was found in a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fennel Whole Seed was packaged in a clear plastic bag Recalled by Mountain...
The Issue: Fennel Whole Seed is recalled due to a potential for contamination with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: IGuide System Recalled by Medical Intelligence Medizintechnik Gmbh Due to...
The Issue: Sometimes, although the HexaPOD has reached the target position, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow AGB+ Multi-Lumen CVC Kit-catheter permits venous access to central...
The Issue: Arrow AGB+ Multi-Lumen CVC Kit - lidstock incorrectly states within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max MRSA Recalled by Becton Dickinson & Co. Due to The foil bags...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Petfine Auto Injector Recalled by Owen Mumford USA, Inc. Due to There is a...
The Issue: There is a possible assembly error on Autoject EI, lot number V14. This lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max Enteric Parasite Panel EU Recalled by Becton Dickinson & Co. Due...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max GC RT PCR Assay Recalled by Becton Dickinson & Co. Due to The...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max ExK DNA 1 USA Recalled by Becton Dickinson & Co. Due to The foil...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit EXT Enteric Bacterial Panel Recalled by Becton Dickinson & Co. Due to...
The Issue: The foil bags containing extraction tubes for BD MAX" Reagent products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.