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. 2,465 recalls have been distributed to Mississippi in the last 12 months.
Showing 24761–24780 of 28,172 recalls
Recalled Item: steroEOS Workstation with software versions: 1.3 Recalled by EOS Imaging Due...
The Issue: Error copying information to the clinical file and to the report when two 3D...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carescape Patient Data Module The Patient Data Module Recalled...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...
The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Interlink threaded lock cannula This is a locking blunt Recalled by...
The Issue: BD Interlink Threaded Lock Cannula REF# 303369 and lot #3021392 is being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Secure II Med/Surg Bed Secure II and the 3002 S3 Recalled by Stryker Medical...
The Issue: Stryker Medical has identified a potential issue associated with Secure II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kit Recalled by Integra LifeSciences Corp. d.b.a....
The Issue: Integra LifeSciences is voluntarily recalling any unexpired lots of HITHSP10...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InstaTrak¿ 3500 Plus Recalled by GE OEC Medical Systems, Inc Due to GE OEC...
The Issue: GE OEC Medical Systems Inc is recalling InstaTrak¿ 3500 Plus, ENTrakTM Plus,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Acetabular Screw 6.5mmx35mm Part Number: 010001000 Recalled by Biomet,...
The Issue: Investigation identified that the outer label, inner label, and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S3 Med/Surg Bed Secure II and the 3002 S3 are Recalled by Stryker Medical...
The Issue: Stryker Medical has identified a potential issue associated with Secure II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthofix Firebird Spinal Fixation System Instrumentation Modular Screw...
The Issue: Orthofix received 6 complaints which resulted in a reportable events due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Camino Advanced Monitor with Waveform Display Model CAM01 Integra...
The Issue: Integra became aware through a complaint from a single non-US customer that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: outer box: Recalled by Biomet, Inc. Due to Inner label of PN: 906768 Lot:...
The Issue: Inner label of PN: 906768 Lot: 055450 CurvTek Eye Needle 22mm X-Large states...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Viscocel and Viscocel Plus. These products are intraocular fluid devices...
The Issue: CLR Medicals International Inc., initiated a nationwide recall of Viscocel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX-Evolution with CSH WS These products are permanently installed...
The Issue: Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integrity. Version 1.1 of the Integrity interface and control software...
The Issue: During the treatment table, gantry, and collimator calibration procedures,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Port Kit with Access Infusion Set under the following labels: Recalled by...
The Issue: Navilyst Medical has recalled a Port Kit with Access Infusion Set due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DR 7500 with FF WS These products are permanently installed Recalled by...
The Issue: Carestream Health Inc. has issued a recall for the Carestream DRX-Evolution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synergy XVI XVI can incorrectly calculate the target position of Recalled by...
The Issue: XVI can incorrectly calculate the target position of the treatment table.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agility. Version 3.1 of the Integrity interface and control software...
The Issue: During the treatment table, gantry, and collimator calibration procedures,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Agility. Version 3.0 of the Integrity interface and control software...
The Issue: During the treatment table, gantry, and collimator calibration procedures,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.