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. 2,419 recalls have been distributed to Colorado in the last 12 months.
Showing 43881–43900 of 51,434 recalls
Recalled Item: Coaxial Micro-Introducer Kit. Greatbatch Part Number/Bard Access Systems...
The Issue: Greatbatch identified that the documentation does not support the five-year...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PediaCare brand NIGHTTIME MULTI-SYMPTOM Cold Recalled by Prestige Brands...
The Issue: Presence of Precipitate; small amounts of diphenhydramine precipitated out...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PediaCare brand DAY & NIGHT Value Pack DAYTIME MULTI-SYMPTOM Cold Recalled...
The Issue: Presence of Precipitate; small amounts of diphenhydramine precipitated out...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: REDVINES FRUIT VINES Bites Cherry ARTIFICIALLY FLAVORED NET WT Recalled by...
The Issue: The nutritional panel on the packaging incorrectly states the sodium content...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: REDVINES FRUIT VINES Bites Strawberry ARTIFICIALLY FLAVORED NET WT Recalled...
The Issue: The nutritional panel on the packaging incorrectly states the sodium content...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Private Selection Chocolate Hazelnut Mascarpone Ice Cream Recalled by Kroger...
The Issue: The firm discovered that the label for two of their products did not declare...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Private Selection Caramel Hazelnut Fudge Truffle Ice Cream Recalled by...
The Issue: The firm discovered that the label for two of their products did not declare...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Oasis Coil Extension Cable used with Hitachi Oasis MRI System Recalled by...
The Issue: The firm received a complaint stating the Coil Extension Cable accessory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation software version 4.0.3.4 RayStation is a software system designed...
The Issue: This notice concerns a problem with the computation of ROI voxel volumes for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BG3515-5 US 5mL BioGlue Surgical Adhesive. BioGlue Surgical Adhesive...
The Issue: Serum albumin component monomer failed to meet internally established end of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revision K Actuator Test Boards sold as replacement parts for Recalled by...
The Issue: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008T Hemodialysis Machine with Revision K Actuator Test Boards...
The Issue: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Famotidine Injection 20 mg Recalled by Baxter Healthcare Corp. Due to...
The Issue: Presence of Particulate Matter: Baxter Healthcare Corporation has received a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...
The Issue: Failed Tablet/Capsule Specifications: Recall due to complaints of split or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...
The Issue: Failed Tablet/Capsule Specifications: Recall due to complaints of split or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Baxter Amia Automated PD systems are used in the treatment Recalled by...
The Issue: System error 01779 is produced when the battery cannot be charged due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UPGRD PRGM 9734638 ADD AxiEM NAVIGATION Recalled by Medtronic Navigation,...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRAPE 9732722 TUBE STERILE O-ARM 20PK Recalled by Medtronic Navigation, Inc....
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUMOR RES. PACK 9733553 AxiEM S.M. Recalled by Medtronic Navigation, Inc....
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KIT Recalled by Medtronic Navigation, Inc. Due to Medtronic Navigation is...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.