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 2194121960 of 28,172 recalls

Medical DeviceApril 29, 2015· HeartWare Inc

Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #: 1101 Recalled by...

The Issue: Complaints with the HVAD Retraction of Pins within the driveline connector.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 29, 2015· HeartWare Inc

Recalled Item: HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac...

The Issue: Complaints with the HVAD Discolored and Cracked Driveline Outer Sheath.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2015· HeartWare Inc

Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and...

The Issue: HeartWare has received complaints relating to damage or bent connection pins...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 29, 2015· HeartWare Inc

Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and...

The Issue: Complaints with the HVAD Internal Controller Alarm Battery failures.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 28, 2015· Alcon Research, Ltd.

Recalled Item: The Alcon Custom Pak. The Alcon Customer Pak is an Recalled by Alcon...

The Issue: The supplier of the Devon Light Glove, a component of the Alcon Custom PAK,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2015· Fresenius Medical Care Holdings, Inc.

Recalled Item: CRIT-LINE Blood Chamber- an accessory to the Crit line III- Recalled by...

The Issue: Blood chamber connection leaks during the use of the CRIT-LINE¿ Blood Chamber

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2015· DeRoyal Industries Inc

Recalled Item: Custom Surgical Kits containing Medtronic Covidien Devon(TM) Light Gloves:...

The Issue: Surgical kits contain Medtronic Covidien Devon(TM) Light Gloves which were...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: EliteCore Full Core Biopsy Device. EliteCore 18G Recalled by Stryker...

The Issue: Potential for the device cannula to overthrow past the intended length.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2015· GE Healthcare

Recalled Item: D-fend Recalled by GE Healthcare Due to A potential safety issue due to loss...

The Issue: A potential safety issue due to loss of gas monitoring associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2015· Philips Medical Systems, Inc.

Recalled Item: Pinnacle3 Software Version 10.0 Recalled by Philips Medical Systems, Inc....

The Issue: A problem (the dose computed in planning mode is calculated incorrectly )...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2015· Covidien LLC

Recalled Item: Palindrome SI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x Recalled by...

The Issue: Catheters may not meet antimicrobial specification

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2015· Covidien LLC

Recalled Item: Palindrome Precision SI Chronic Catheter Sport Pack w/VenaTrac Stylet 14.5...

The Issue: Catheters may not meet antimicrobial specification

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2015· Covidien LLC

Recalled Item: Palindrome Precision SI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr...

The Issue: Catheters may not meet antimicrobial specification

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2015· Covidien LLC

Recalled Item: Palindrome SI Chronic Catheter Sport Pack 14.5 Fr x 33 cm Item Code:...

The Issue: Catheters may not meet antimicrobial specification

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2015· Covidien LLC

Recalled Item: Palindrome SI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x Recalled by...

The Issue: Catheters may not meet antimicrobial specification

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2015· Covidien LLC

Recalled Item: Palindrome Precision SI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr...

The Issue: Catheters may not meet antimicrobial specification

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2015· Covidien LLC

Recalled Item: Palindrome SI Chronic Catheter Sport Pack w/VenaTrac Stylet 14.5 Fr Recalled...

The Issue: Catheters may not meet antimicrobial specification

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2015· Covidien LLC

Recalled Item: Palindrome Precision HSI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr...

The Issue: Catheters may not meet antimicrobial specification

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2015· Covidien LLC

Recalled Item: Palindrome HSI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x Recalled by...

The Issue: Catheters may not meet antimicrobial specification

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 23, 2015· Covidien LLC

Recalled Item: Palindrome Precision HSI Chronic Catheter Sport Pack w/VenaTrac Stylet 14.5...

The Issue: Catheters may not meet antimicrobial specification

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

Class II — Potential Health HazardOngoing