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. 2,538 recalls have been distributed to Colorado in the last 12 months.
Showing 21901–21920 of 51,434 recalls
Recalled Item: Merge OrthoPACS versions 7.3 Recalled by Merge Healthcare, Inc. Due to...
The Issue: Potential for prior thumbnails to not display in reverse chronological order...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS versions 7.3 Recalled by Merge Healthcare, Inc. Due to Potential...
The Issue: Potential for prior thumbnails to not display in reverse chronological order...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equate Night-time Sleep Aide (Diphenhydramine HCl) Recalled by LNK...
The Issue: Microbial contamination of non-sterile product
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IMMULITE 1000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: There is a potential for low discordant progesterone results on a subset of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX Analyzer UDI:05700693930909 Recalled by Radiometer America Inc...
The Issue: Software Security; The action is being initiated because of software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: There is a potential for low discordant progesterone results on a subset of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drospirenone and Ethinyl Estradiol Tablets Recalled by Jubilant Cadista...
The Issue: Failed dissolution specifications : failed results at the 3-month stability...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dolfin Dark Chocolate with Pink Peppercorns Net Wt 2.47 oz (70g) Recalled by...
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PROBAR MEAL Superfood Slam Recalled by Probar LLC Due to Undeclared Milk
The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PROBAR The Simply Real Bar: Chocolate Coconut Recalled by Probar LLC Due to...
The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PROBAR MEAL Original Trail Mix Recalled by Probar LLC Due to Undeclared Milk
The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PROBAR MEAL Peanut Butter Chocolate Chip Recalled by Probar LLC Due to...
The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PROBAR MEAL Chocolate Coconut Recalled by Probar LLC Due to Undeclared Milk
The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PROBAR MEAL Wholeberry Blast Recalled by Probar LLC Due to Undeclared Milk
The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is Recalled by...
The Issue: code 7-102 Liquid Sensor Error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643...
The Issue: Potential of an open port in the quench venting system when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Prisma magnetic resonance diagnostic devices Model #10849582...
The Issue: Potential of an open port in the quench venting system when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Skyra magnetic resonance diagnostic devices Model # 10432915...
The Issue: Potential of an open port in the quench venting system when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914...
The Issue: Potential of an open port in the quench venting system when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gablofen (baclofen injection) Recalled by Piramal Critical Care, Inc. Due to...
The Issue: Failed Impurities/Degradation Specification -This recall is being initiated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.