Product Recalls in Montana
Product recalls affecting Montana — including food, drugs, consumer products, medical devices, and vehicles distributed to Montana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,989 recalls have been distributed to Montana in the last 12 months.
Showing 4361–4380 of 27,852 recalls
Recalled Item: Sterile surgical convenience kit: Medline Retrograde PK-22025203-LF Recalled...
The Issue: Surgical convenience kits containing Pure Pouch component that has weak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile convenience kits: a. Medline CC Drawer 4 IV Circulation Recalled...
The Issue: Surgical convenience kits containing Pure Pouch component that has weak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioZorb Marker-BioZorb 3D Bioabsorbable Marker-Intended Use radiographic...
The Issue: Safety Information: Complaints describe complications/adverse events that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: CLEANER BOTTLE Product Name: CLEANER BOTTLE Model/Catalog...
The Issue: Received complaints that bottles assembled with one batch of bottle collars...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: WATER BOTTLE Product Name: WATER BOTTLE Model/Catalog Number:...
The Issue: Received complaints that bottles assembled with one batch of bottle collars...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: PIEZON Bottle Product Name: PIEZON Bottle Model/Catalog Number:...
The Issue: Received complaints that bottles assembled with one batch of bottle collars...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Knee System AS Tibial Bearing / DCM ArCom Recalled by Biomet, Inc....
The Issue: Possible damage to the Vanguard Knee System AS Tibial Bearing caused during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Iron3 - IVD use in the quantitative measurement Recalled by...
The Issue: Potential for falsely elevated Chol_2, LDLC, and Trig_2 results on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Omni/Stellar Recalled by Philips North America Llc Due to...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Master/Nova 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: Intera Achieva 1.5T Pulsar Recalled by Philips North America Llc Due to...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolution Upgrade 3.0T 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 1.5T Conversion 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: Enterprise 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: Ingenia Elition X 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: Intera 1.0T Power/Pulsar Recalled by Philips North America Llc Due to...
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 CONVENIENCE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Products have a lack of sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T Recalled by Philips North America Llc Due to...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Explorer/Nova Dual Recalled by Philips North America Llc Due to...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.