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. 2,489 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,489 in last 12 months

Showing 2128121300 of 28,172 recalls

Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: Immutest 10 Pnl Drug Screen Cup w/ Adult Recalled by Ameditech Inc Due to...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: ProScreen 10 Drug Panel Cassette Test Recalled by Ameditech Inc Due to...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: The Drug Detection Agency 6 Panel Cup Body and Lid w/Adult (AU) Recalled by...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: Premier Clia Waived 12 panel Tilt Cup Recalled by Ameditech Inc Due to...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: DrugCheck Pipette 10 Drug Test Recalled by Ameditech Inc Due to Ameditech is...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: 1 Step 12 Panel Cup Recalled by Ameditech Inc Due to Ameditech is recalling...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: 11 Panel Dip Card (OPI 2000) Recalled by Ameditech Inc Due to Ameditech is...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: DrugCheck Waived 12 Panel Cup w/Adult Recalled by Ameditech Inc Due to...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2015· Bard Peripheral Vascular Inc

Recalled Item: FLAIR Endovascular Stent Graft Recalled by Bard Peripheral Vascular Inc Due...

The Issue: Bard Peripheral Vascular (BPV) is recalling the Bard Flair Endovascular...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2015· Invivo Corporation

Recalled Item: The system provides the ability to transmit patient data files for storage...

The Issue: Display of SpO2 and Non-Invasive Blood Pressure (NIBP) Measurements May Freeze

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2015· Arrow International Inc

Recalled Item: ARROW PICC Kit featuring Chlorag+ard Technology Midline Catheterization Kit...

The Issue: Possibility that the catheter peel-away component hub tabs may prematurely...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2015· Utah Medical Products, Inc

Recalled Item: Myelo-Nate CSF Sampling Kit Recalled by Utah Medical Products, Inc Due to...

The Issue: Utah Medical is conducting a recall of Myelo-Nate CSF Sampling Kit due to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2015· Euro Diagnostica AB

Recalled Item: DIASTAT anti-Nuclear antibody (ANA) / DIASTAT ANA ELISA. Catalog Number:...

The Issue: Complaint investigation concluded that although product quality requirements...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Philips Electronics North America Corporation

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Electronics...

The Issue: The following MRx software issue has been identified: MRx model M3535A with...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Covidien LLC

Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...

The Issue: Incorrectly packaged with a 90 degree bend at the distal tip

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Covidien LLC

Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...

The Issue: Incorrectly packaged with a 90 degree bend at the distal tip

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Covidien LLC

Recalled Item: Palindrome" Chronic Catheter Kit Symmetrical Tip Recalled by Covidien LLC...

The Issue: Incorrectly packaged with a 90 degree bend at the distal tip

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Stryker Sustainability Solutions

Recalled Item: SSS Reprocessed Zimmer Recalled by Stryker Sustainability Solutions Due to...

The Issue: It was reported that packaging was not properly sealed.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Covidien LLC

Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...

The Issue: Incorrectly packaged with a 90 degree bend at the distal tip

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Covidien LLC

Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip 14.5 Fr/Ch (4.8mm)...

The Issue: Incorrectly packaged with a 90 degree bend at the distal tip

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

Class II — Potential Health HazardOngoing