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. 1,065 recalls have been distributed to Colorado in the last 12 months.
Showing 16541–16560 of 51,434 recalls
Recalled Item: VIDAS¿ CMV IgM 30 Tests Recalled by Biomerieux Inc Due to bioMerieux...
The Issue: bioMerieux received complaints about calibration issue observed on several...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD UF PEN 32GX4MM 100 NANO Item Number: 4292272 Recalled by Cardinal Health...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONETOUCH DELICA LANCETS 30G 100 COUNT Item Number: 5541610 Recalled by...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5" (13 cm) Bag Spike Adapter w/Spiros" w/Red Cap Recalled by ICU Medical,...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spiros Closed Male Luer - Product Usage: provides Recalled by ICU Medical,...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 670G Insulin Pump: Models: PUMP MMT-1740KX 670G V6.3 SF MG CLIN...
The Issue: Due to a software design issue, under certain conditions, a software fault...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 780G Insulin Pump: Models: PUMP MMT-1885 MM780G 6.5V BLE MMOL...
The Issue: Due to a software design issue, under certain conditions, a software fault...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Filtered Triple-Leg Extension Set - Intravascular administration set....
The Issue: BBMI has identified through complaints the potential for the extension set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDURITY Pulse Generator **** SN ********* St. Jude Medical Recalled by St....
The Issue: Due to a manufacturing issue associated with the mixing process of the epoxy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASSURITY Pulse Generator **** SN ********* ST. JUDE MEDICAL Recalled by St....
The Issue: Due to a manufacturing issue associated with the mixing process of the epoxy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diluent Recalled by Medline Industries Inc Due to Possible false negative or...
The Issue: Possible false negative or false positive results due to the product being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nuts.com brand Diced Dried Figs packaged in 1lb stand up gusset pouches....
The Issue: Undeclared almonds in diced fig product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ZOMA-Jet 5 Demonstration Kit Recalled by Ferring Pharmaceuticals Inc Due to...
The Issue: Defective Delivery System: customer complaints concerning the injector pen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl Injection Recalled by Sagent Pharmaceuticals Inc Due to...
The Issue: Lack of Assurance of Sterility: customer complaints of loose crimped vial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Omeprazole Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: Failed Impurities/Degradation Specifications: Out-of-Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZOMA-Jet 10 Demonstration Kit Recalled by Ferring Pharmaceuticals Inc Due to...
The Issue: Defective Delivery System: customer complaints concerning the injector pen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tibial Opening Wedge Osteotomy Plate Recalled by Arthrex, Inc. Due to It was...
The Issue: It was discovered that five AR-13200ST-15.0 parts were processed as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydraVision Digital Imaging System Product ID/Reorder Number: 705559 (65KW)...
The Issue: Failure to comply with the performance standard for fluoroscopy systems. Per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tritanium X TL Instruments - intervertebral fusion device with bone graft...
The Issue: Stryker identified non-conforming instruments that are components of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Haemophilus Test Medium (150 mm) 10/PK Recalled by Remel Inc Due to...
The Issue: When tested with H. influenza ATCC 49247 and ATCC 49766 both organisms may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.