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. 2,411 recalls have been distributed to Mississippi in the last 12 months.
Showing 40521–40540 of 49,744 recalls
Recalled Item: GENTAMICIN INJECTION Recalled by Fresenius Kabi USA, LLC Due to Defective...
The Issue: Defective Container: Vials may be missing stoppers.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Beachbody Hardcore Base Shake Lot #42932B22 Recalled by Beachbody Llc Due to...
The Issue: During an investigation of label issuance and reconciliation at the firm's...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Caviar Medley/Garden Vegetable 12/36 oz Product number 10610 Recalled by...
The Issue: Firm was notified by supplier of Garden Vegetable Seasoning that the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Garden Vegetable seasoning Mix 12/4 oz. Product number 141000 Garden...
The Issue: Firm was notified by supplier of Garden Vegetable Seasoning that the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Whole Grain 5 Blend/Garden Vegetable 12/36 oz Product number 12410 Recalled...
The Issue: Firm was notified by supplier of Garden Vegetable Seasoning that the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Rio Medley/Garden Vegetable 12/36 oz Recalled by InHarvest, Inc. Due to Firm...
The Issue: Firm was notified by supplier of Garden Vegetable Seasoning that the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: White and Wild Medley/Garden Vegetable 12/36 oz Recalled by InHarvest, Inc....
The Issue: Firm was notified by supplier of Garden Vegetable Seasoning that the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ADULT Radiotranslucent Electrode Recalled by Heart Sync, Inc. Due to Heart...
The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Single-Use Curved Jewelers/Iris Bipolar Forceps Sterile RX Recalled by...
The Issue: The product is sold and labeled as EO sterilized, however the units were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlignRT is a video-based three-dimensional (3D) surface imaging system which...
The Issue: Potential use error when the external Gate Controller is turned ON after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Printouts...
The Issue: Printouts may be printed in incorrect anatomical size when using syngo.plaza...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT/CHILD Radiotransparent Electrode Recalled by Heart Sync, Inc. Due to...
The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT/CHILD Radiotranslucent Electrode Recalled by Heart Sync, Inc. Due to...
The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT Radiotranslucent Electrode Recalled by Heart Sync, Inc. Due to Heart...
The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solitaire-C Cervical Spacer System a) 14-531593 Drill/Awl Sleeve b)...
The Issue: A design deficiency was discovered whereby the Drill/Awl Sleeve and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pediatric Recalled by Cure Medical LLC Due to Some of the intermediate boxes...
The Issue: Some of the intermediate boxes within lot 140417-3, were labeled as P8, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT Radiotransparent Electrode Recalled by Heart Sync, Inc. Due to Heart...
The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Nerve Block Component Recalled by Arrow International Inc Due to Arrow...
The Issue: Arrow is recalling certain lots of the Continuous Nerve Block Component,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rotating Tibial Platform ATTUNE INTUITION Impactor. The ATTUNE INTUITION...
The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fixed Tibial bearing ATTUNE INTUITION Impactor The ATTUNE INTUITION...
The Issue: ATTUNE INTUITION Impactors (cat. nos. 254401003, 254401004, and 254401006)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.