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. 2,617 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,617 in last 12 months

Showing 1120111220 of 28,172 recalls

Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 30"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 0 Undyed 36"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 2/0 Undyed 30"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 30"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 18"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 4/0 Undyed 30"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 36"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 3/0 Undyed 30"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2020· Riverpoint Medical, LLC

Recalled Item: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 1 Undyed 36"...

The Issue: The surgical suture is non-sterile. Use could compromise the sterile field,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2020· MicroPort Orthopedics Inc.

Recalled Item: PROFEMUR Titanium and Cobalt Chrome modular necks Recalled by MicroPort...

The Issue: MicroPort Orthopedics Inc. is voluntarily recalling any existing inventory...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2020· Klarity Medical Products LLC

Recalled Item: Klarity Vacuum Bags Recalled by Klarity Medical Products LLC Due to Vacuum...

The Issue: Vacuum bags potentially may not hold their vacuum adequately for needed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· Thera Test Laboratories, Inc.

Recalled Item: EL-Anti-SARS-CoV-2 IgM Kit Recalled by Thera Test Laboratories, Inc. Due to...

The Issue: Device did not meet the updated EUA packet requirements for positive percent...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump - T34 - Product Usage: infusion Recalled by CME...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump - T34L PCA - Product Usage: Recalled by CME...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump - Neofeed - Product Usage: infusion Recalled by...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump - Ameritus 1st Enteral Pump - Recalled by CME...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump - NeoThrive - Product Usage: infusion Recalled by...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· CME America, LLC

Recalled Item: CME America T-Syringe Pump -T34L - Product Usage: infusion of Recalled by...

The Issue: Multiple reasons: 1) Due to wear and tear of pump motor block mechanism -...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2020· Cardinal Health 200, LLC

Recalled Item: KIT Recalled by Cardinal Health 200, LLC Due to Only providing one nasal...

The Issue: Only providing one nasal swab in our pre-operative kit instead of the 4...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2020· Sorin Group Italia S.r.l.

Recalled Item: Perceval Single Use Accessory Kit Recalled by Sorin Group Italia S.r.l. Due...

The Issue: LivaNova received complaints indicating the impossibility to collapse...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing