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 3441–3460 of 49,744 recalls
Recalled Item: Progesterone Injection USP Recalled by Eugia US LLC Due to Presence of...
The Issue: Presence of Particulate Matter: A market complaint was received of a glass...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prograf (tacrolimus) capsules Recalled by Astellas Pharma US Inc. Due to...
The Issue: Failed Tablet/Capsule Specifications: Bottles shipped to the USA may contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Astagraf XL (tacrolimus extended-release capsules) 0.5 mg Recalled by...
The Issue: Failed Tablet/Capsule Specifications: Bottles shipped to the USA may contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: First Aid Beauty Ultra Repair Cream Recalled by First Aid Beauty Ltd Due to...
The Issue: CGMP Deviations; product intended for quarantine was inadvertently distributed
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardura XL (doxazosin) extended release tablets 8 mg Recalled by Viatris Inc...
The Issue: Failed Impurities/Degradation Specifications: Out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardura XL (doxazosin) extended release tablets 4 mg Recalled by Viatris Inc...
The Issue: Failed Impurities/Degradation Specifications: Out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AnchorFast SlimFit Recalled by Hollister Incorporated Due to Hollister...
The Issue: Hollister received reports of decreased skin barrier wear time which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnchorFast Recalled by Hollister Incorporated Due to Hollister received...
The Issue: Hollister received reports of decreased skin barrier wear time which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnchorFast Guard Select Recalled by Hollister Incorporated Due to Hollister...
The Issue: Hollister received reports of decreased skin barrier wear time which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AnchorFast Guard Recalled by Hollister Incorporated Due to Hollister...
The Issue: Hollister received reports of decreased skin barrier wear time which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyberKnife Treatment Delivery System Recalled by Accuray Incorporated Due to...
The Issue: Snap rings may become partially or completed detached from the shafts within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VDR4 Phasitron Breathing Circuit Models that contain the venturi component:...
The Issue: Due to internal venturi component getting transiently stuck in the forward...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adrenalin Chloride Solution (Epinephrine Nasal Solution Recalled by ENDO...
The Issue: Labeling: Not Elsewhere Classified: misleading label similar in appearance...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...
The Issue: Due to faulty circuit board in speed control remote use in conjunction with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...
The Issue: Due to faulty circuit board in speed control remote use in conjunction with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLENE Polypropylene Suture Recalled by Ethicon, LLC Due to Sutures may...
The Issue: Sutures may have an open seal on the primary packaging, due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHIBOND EXCEL Polyester Suture Recalled by Ethicon, LLC Due to Sutures may...
The Issue: Sutures may have an open seal on the primary packaging, due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERMA-HAND Silk Suture Recalled by Ethicon, LLC Due to Sutures may have an...
The Issue: Sutures may have an open seal on the primary packaging, due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOS Stent and Delivery System 10mmx10mm UPN: M00553740 Recalled by Boston...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 10mmx10mm UPN:...
The Issue: Reported Outer sheath distal black tip detaching from the device can remain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.