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. 2,489 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,489 in last 12 months

Showing 3386133880 of 51,434 recalls

Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Curved Spatula Electrode 28CM Item Code: E278128 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Curved Spatula Electrode Retractable 28CM Item Code:...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Argon Sharp Needle Electrode 28CM Item Code: E258228...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Straight Spatula Electrode 36C Item Code: E277036 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic AP Argon Blunt Needle Electrode 28cm Item Code:...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Flexible Laparoscopic Argon Electrodes 6" Item Code:...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2016· TZ Medical, Inc.

Recalled Item: Neptune Plus (Hemostatic Pad) Recalled by TZ Medical, Inc. Due to Neptune...

The Issue: Neptune Plus was mis-labeled and included the statement WITH ANTIMICROBIAL...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2016· Philips Electronics North America Corporation

Recalled Item: Allura Xper with release R8.2: Allura Xper FD10 Recalled by Philips...

The Issue: Increase in the failure rate of certain low-voltage DC power supplies (DCPS)

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2016· Philips Electronics North America Corporation

Recalled Item: UNIQ 1.0: UNIQ FD10 Recalled by Philips Electronics North America...

The Issue: Increase in the failure rate of certain low-voltage DC power supplies (DCPS)

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/ zeego Recalled by Siemens Medical Solutions USA, Inc Due to Due...

The Issue: Due to an error in the 19 Live Display, image reproduction may fail in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2016· Arrow International Inc

Recalled Item: Walrus Arterial Embolectomy Catheter The arterial embolectomy catheter is...

The Issue: Arrow is recalling due to incorrect labeling of products.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2016· Zimmer Trabecular Metal Technology, Inc.

Recalled Item: The TM Ardis Interbody System implant is a convex Recalled by Zimmer...

The Issue: This field action is being initiated following the firm's discovery of a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
FoodJuly 7, 2016· Newly Weds Foods Inc

Recalled Item: Bulk packaged flour based "breader" packaged in 25 Recalled by Newly Weds...

The Issue: The supplier received flour from General Mills that was contaminated with E....

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 7, 2016· Continental Mills (Corporate Office)

Recalled Item: Krusteaz Blueberry Pancake Mix Recalled by Continental Mills (Corporate...

The Issue: Krusteaz Blueberry Pancake Mix is recalled due to a potential to be...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 7, 2016· Newly Weds Foods Inc

Recalled Item: Bulk packaged flour based tortilla bits packaged in 45.5 lb. bags. Recalled...

The Issue: The supplier received flour from General Mills that was contaminated with E....

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 6, 2016· Kabobs Inc

Recalled Item: VEGETABLE EMPANADA Recalled by Kabobs Inc Due to Potential E. coli Contamination

The Issue: Product was manufactured with flour recalled due to E. coli O121 contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2016· Kabobs Inc

Recalled Item: MINI CLASSIC FRENCH QUICHE Recalled by Kabobs Inc Due to Potential E. coli...

The Issue: Product was manufactured with flour recalled due to E. coli O121 contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2016· Kabobs Inc

Recalled Item: MINI VEGETABLE SPRINGROLL Recalled by Kabobs Inc Due to Potential E. coli...

The Issue: Product was manufactured with flour recalled due to E. coli O121 contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2016· Kabobs Inc

Recalled Item: SHRIMP SPRINGROLL Recalled by Kabobs Inc Due to Potential E. coli Contamination

The Issue: Product was manufactured with flour recalled due to E. coli O121 contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 6, 2016· Kabobs Inc

Recalled Item: COCONUT LOBSTER TAIL Recalled by Kabobs Inc Due to Potential E. coli...

The Issue: Product was manufactured with flour recalled due to E. coli O121 contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund