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. 2,509 recalls have been distributed to Colorado in the last 12 months.
Showing 28381–28400 of 51,434 recalls
Recalled Item: Variety Pack Organic Recalled by San Gennaro Foods, Inc Due to Date coding...
The Issue: Date coding ink was being printed directly on the food contact surface of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clofarabine injection Recalled by Sanofi-Aventis U.S. LLC Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Package Insert: authorized generic product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clolar (clofarabine) 20 mg/20 mL (1 mg/mL) Injection Recalled by Genzyme...
The Issue: Labeling: Incorrect or Missing Package Insert.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carestation 620 A2 Recalled by GE Medical Systems China Co., Ltd. Due to...
The Issue: Possible incomplete seal between the CO2 absorber and the breathing circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestation 620 A1 Recalled by GE Medical Systems China Co., Ltd. Due to...
The Issue: Possible incomplete seal between the CO2 absorber and the breathing circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental Tapered SwissPlus & SwissPlus Implant Systems surgical kit...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental Instrument Kit System Recalled by Zimmer Dental Inc Due to The...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental Instrument Kit System Recalled by Zimmer Dental Inc Due to The...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TunneLoc Tibial Fixation Device (Within an ACL Kit) Product Usage: Recalled...
The Issue: Gamma sterilization validation testing indicates the sterilization dose for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Dental GemLock RHD2.5 Hex Driver. The label shows the Recalled by...
The Issue: The device may contain a manufacturing condition affecting the geometry of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TunneLoc Tibial Fixation Device Product Usage: To provide fixation of...
The Issue: Gamma sterilization validation testing indicates the sterilization dose for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arkon Anesthesia Delivery System Recalled by Spacelabs Healthcare, Ltd. Due...
The Issue: Arkon Anesthesia Workstation, with software version 2.61, experienced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STORZ High Flow Insufflation Tubing (with filter) Recalled by Karl Storz...
The Issue: The label outside the cardboard box is labeled correctly but the pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect Legacy(TM) 3 Implant Recalled by Implant Direct Sybron...
The Issue: One reported complaint and discovered that the outer vial was out of round...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crimson Trace Corporation laser sights. The Finished Products are laser...
The Issue: A previously "in specification" Finished Product with a Model 25-0657 diode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: La Terra Fina Spinach Artichoke & Parmesan Dip & Spread Recalled by La Terra...
The Issue: Undeclared allergen; egg.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VANCOmycin 1.25 grams added to 0.9% Sodium Chloride 500 mL bag Recalled by...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone HCl 10 mg (0.2mg/ml) 50 mL syringes in 0.9% Sodium Chloride...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Midazolam HCL 100 mg (1mg/mL) 100 mL Cassette in 0.9% Sodium Chloride...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ropivacaine HCL (PF) 0.2% (2mg/mL) 100 mL Cassette Rx Only Recalled by...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.