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. 2,551 recalls have been distributed to Colorado in the last 12 months.
Showing 19921–19940 of 51,434 recalls
Recalled Item: Bard Biopsy EnCor Probe Recalled by Bard Peripheral Vascular Inc Due to Lot...
The Issue: Lot numbers and products inadvertently not included in the scope of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Sterile Disposable Tourniquet Cuff with Protective Sleeve and PLC...
The Issue: When inflating/deflating a single bladder, both bladders could potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coated VICRYL (Polyglactin 910) Suture Recalled by Ethicon, Inc. Due to Some...
The Issue: Some sutures in the lot may exhibit a small section of braid fraying, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medonic M-Series Hematology Analyzer M16S BD ABR US Product code: 1400075...
The Issue: A mix-up of autosampler tube positions with a possibility of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integris Allura 9 Recalled by Philips North America, LLC Due to A capacitor...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardio Vascular-Allura Centron Recalled by Philips North America, LLC Due to...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroDiagnost Eleva Recalled by Philips North America, LLC Due to A capacitor...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniDiagnost Eleva System codes 708028 708027 Recalled by Philips North...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integris Allura 15 & 12 Recalled by Philips North America, LLC Due to A...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnost Eleva Recalled by Philips North America, LLC Due to A...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Poly G Integris H5000 Recalled by Philips North America, LLC Due to A...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura CV20 Recalled by Philips North America, LLC Due to A capacitor inside...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Exper FD Series. System codes 722003 722010 722022 722005 Recalled by...
The Issue: A capacitor inside the converter of the Velara X-ray generator may fail...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TwinFix Ti 2.8 mm HS Suture Anchor - Product Usage: Recalled by Smith &...
The Issue: Due to a potential for sterile barrier breach. A complaint was received that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dawson-Mueller Drainage Catheter Recalled by Cook Inc. Due to Specific lots...
The Issue: Specific lots of the Dawson-Mueller Drainage Catheter were not manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proparacaine Hydrochloride Ophthalmic Solution Recalled by Akorn, Inc. Due...
The Issue: Chemical contamination; out of specification results obtained for equipment...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blisovi Fe 1.5/30 (norethindrone acetate and ethinyl estradiol tablets USP...
The Issue: Failed Tablet/Capsule Specifications: Complaints related to crumbling of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cece's Veggie Co. brand Fresh Veggie Ramen with Chicken Broth (11.5 oz...
The Issue: Potential to be contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SimplySafe Sesame Seed Hulled Recalled by Bay State Milling Co. Due to...
The Issue: Product may be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Prometra II 20mL Pump. Catalog No. 13827 The device is Recalled by Flowonix...
The Issue: A pump alarm function anomaly in the pump firmware code may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.