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. 1,099 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
1,099 in last 12 months

Showing 15201–15220 of 51,434 recalls

Medical DeviceAugust 10, 2021· DePuy Orthopaedics, Inc.

Recalled Item: TRUMATCH CT CUT GUIDE FEM L- TruMatch Patient Specific Instruments Recalled...

The Issue: Software: A coding error associated with the Fast3D Segmentation software....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: 10 drops/ml Recalled by B. Braun Medical, Inc. Due to Leakage of the pump...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· DePuy Orthopaedics, Inc.

Recalled Item: TRUMATCH CT PIN GUIDE FEM R- TruMatch Patient Specific Instruments Recalled...

The Issue: Software: A coding error associated with the Fast3D Segmentation software....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· DePuy Orthopaedics, Inc.

Recalled Item: TRUMATCH CT FEM CUT TIB PIN R- TruMatch Patient Specific Recalled by DePuy...

The Issue: Software: A coding error associated with the Fast3D Segmentation software....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· DePuy Orthopaedics, Inc.

Recalled Item: TRUMATCH CT PIN GUIDE KIT R- TruMatch Patient Specific Instruments Recalled...

The Issue: Software: A coding error associated with the Fast3D Segmentation software....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· DePuy Orthopaedics, Inc.

Recalled Item: TRUMATCH CT CUT GUIDE KIT L- TruMatch Patient Specific Instruments Recalled...

The Issue: Software: A coding error associated with the Fast3D Segmentation software....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: V1500HP OUTLOOK PUMP SET 118-single-use for use with the Outlook Recalled by...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: OUTLOOK PUMP IV SET Recalled by B. Braun Medical, Inc. Due to Leakage of the...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: Outlook Pump Add-On Set-single use Recalled by B. Braun Medical, Inc. Due to...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: OUTLOOK PUMP SET Recalled by B. Braun Medical, Inc. Due to Leakage of the...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2021· Beckman Coulter Inc.

Recalled Item: Access hsTnI High Sensitivity Troponin I Recalled by Beckman Coulter Inc....

The Issue: Through customer feedback, testing a sample with cardiac troponin I...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2021· Ad-Tech Medical Instrument Corporation

Recalled Item: Ad-Tech TECH ATTACH Cable- Product Usage: Designed for the purpose Recalled...

The Issue: Incorrect version of labels were used.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2021· Ad-Tech Medical Instrument Corporation

Recalled Item: Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the Recalled...

The Issue: Incorrect version of labels were used.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2021· Smiths Medical ASD Inc.

Recalled Item: Bivona Aire-Cuf Endotracheal Tube Recalled by Smiths Medical ASD Inc. Due to...

The Issue: Inadequate pouch seal leading to a compromised sterile barrier on products...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2021· Ad-Tech Medical Instrument Corporation

Recalled Item: Ad-Tech Lightweight TECH ATTACH Cable - Product Usage: Designed for Recalled...

The Issue: Incorrect version of labels were used.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2021· Smiths Medical ASD Inc.

Recalled Item: Bivona Uncuffed Wire Endotracheal Tubes Recalled by Smiths Medical ASD Inc....

The Issue: Inadequate pouch seal leading to a compromised sterile barrier on products...

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

Class II — Potential Health HazardOngoing
FoodAugust 7, 2021· Gem City Fine Foods, LLC

Recalled Item: Triple Berry Streusel Cheesecake Recalled by Gem City Fine Foods, LLC Due to...

The Issue: Frozen desserts are mislabeled. Flourless Chocolate Torte mislabeled with...

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

Class III — Low RiskOngoing
Refund
FoodAugust 7, 2021· Gem City Fine Foods, LLC

Recalled Item: Flourless Chocolate Torte Recalled by Gem City Fine Foods, LLC Due to...

The Issue: Frozen desserts are mislabeled. Flourless Chocolate Torte mislabeled with...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing