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. 2,702 recalls have been distributed to Colorado in the last 12 months.
Showing 4481–4500 of 28,964 recalls
Recalled Item: Intera 1.5T R11 Recalled by Philips North America Llc Due to Patient support...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T Recalled by Philips North America Llc Due to Patient support...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Initial Recalled by Philips North America Llc Due to Patient...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0TX for PET Recalled by Philips North America Llc Due to Patient...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Namic FLUID DELIVERY SET Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Products have a lack of sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Recalled by Philips North America Llc Due to Patient support...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OsmoPRO MAX Automated Osmometer- IVD Osmometer for Clinical Use. Uses...
The Issue: System error messages may delay the ability to test patient samples and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HDS Traction Boot II Recalled by Baxter Healthcare Corporation Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENASYS EDGE 300ML CANISTER WITH Solidifier- Indicated for patients who...
The Issue: Black particulate matter from the carbon filter component of the canisters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Identity Imprint PS Tibial Tray Size 4: Lot 540287 Recalled by Conformis,...
The Issue: Size 5 Tibial Tray from Lot 508287 was packaged in a Size 4 box from Lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENASYS EDGE 800ML CANISTER WITH Solidifier- Indicated for patients who...
The Issue: Black particulate matter from the carbon filter component of the canisters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Galaxy System (specifically GAL-019 Recalled by Noah Medical Due to Due to a...
The Issue: Due to a misaligned calibration of the wired controller that may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STRATAFIX Spiral MONOCRYL Plus Bidirectional Knotless Tissue Control Device:...
The Issue: Degraded and unusable upon removal from the foil pouch due to exposed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LVP Software of the Ivenix Infusion System (IIS) Recalled by Fresenius Kabi...
The Issue: Software has anomalies that have the potential to cause underdose, overdose,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...
The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...
The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...
The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...
The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe REVERSE SHOULDER Recalled by Exactech, Inc. Due to The...
The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...
The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.