Product Recalls in Mississippi
Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,661 recalls have been distributed to Mississippi in the last 12 months.
Showing 2201–2220 of 28,172 recalls
Recalled Item: SIGNA MR380 Recalled by GE Healthcare (China) Co., Ltd. Due to For certain...
The Issue: For certain MR systems, a scan can be resumed following a Power Monitor trip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima MR360 Recalled by GE Healthcare (China) Co., Ltd. Due to For certain...
The Issue: For certain MR systems, a scan can be resumed following a Power Monitor trip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Pipeline Vantage Embolization Device with Shield Technology...
The Issue: Use of embolization device with diameters greater-than-or-equal-to 4mm may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Pipeline Vantage Embolization Device with Shield Technology...
The Issue: Use of embolization device with diameters greater-than-or-equal-to 4mm may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Connected Blood Glucose Meter Recalled by Telcare, LLC Due to...
The Issue: Telcare, LLC has received customer complaints related to battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Leica Biosystems Cryostats Product Name: CM1950 Model/Catalog...
The Issue: Firm became aware of software issues related to most recent firmware update...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker CinchLock Flex Knotless Anchor with Inserter and Suture Recalled by...
The Issue: Increase in complaints concerning "pullwire" breakage that may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Medical Video Processor- Intended to be used with PENTAX Recalled by...
The Issue: During endoscopic procedures using a combination of the video processor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTAX Medical Video Upper GI Scope-Intended to provide optical...
The Issue: During endoscopic procedures using a combination of the video processor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTAX Medical Video Colonoscope- Intended to provide optical visualization...
The Issue: During endoscopic procedures using a combination of the video processor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima XR646 HD. X-Ray imaging system. Recalled by GE Medical Systems, LLC...
The Issue: The user can continue to take the next exposure after reaching the Automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Definium 656HD & Discovery XR656HD (GTINs: 00840682138598 Recalled by GE...
The Issue: The user can continue to take the next exposure after reaching the Automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery XR656 HD. X-Ray imaging system. Recalled by GE Medical Systems,...
The Issue: The user can continue to take the next exposure after reaching the Automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery XR656HD. X-Ray imaging system. Recalled by GE Medical Systems, LLC...
The Issue: The user can continue to take the next exposure after reaching the Automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ET Rigid Abutment (Mini) SIze: 4.5D 4.0G/H 4.0H - Intended Recalled by...
The Issue: Patient chart stickers provided inside the packaging may incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Osstem Implant System - Abutment ET Multi Abutment Size: 4.8D Recalled by...
The Issue: Patient chart stickers provided inside the packaging may incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ET Rigid Abutment (Mini) Size 4.5D 1.0G/H 5.0H - Intended Recalled by...
The Issue: Patient chart stickers provided inside the packaging may incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ET Rigid Abutment (Mini) SIze: 4.5D 3.0G/H 7.0H - Intended Recalled by...
The Issue: Patient chart stickers provided inside the packaging may incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ET Rigid Abutment (Mini) Size: 4.5D 2.0G/H 4.0H- Intended for Recalled by...
The Issue: Patient chart stickers provided inside the packaging may incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TISSUE APPROXIMATION SYSTEM (TAS) Recalled by TAS Medical Inc Due to Tissue...
The Issue: Tissue approximation straps (zip-ties) have broken before or during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.