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. 2,476 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,476 in last 12 months

Showing 2370123720 of 28,172 recalls

Medical DeviceJune 17, 2014· Varian Medical Systems, Inc.

Recalled Item: C-Series High Energy Linear Accelerator - Models: Novalis Tx Recalled by...

The Issue: Trend in reports of unexpected decrease in beam output in C-series High...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo¿ Advanced Perfusion System 1 220/240V AC Recalled by Terumo...

The Issue: An evaluation of the APS1 Operator Manual found that existing instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2014· Baxter Healthcare Corp.

Recalled Item: Baxter MiniCap with Povidone-Iodine Solution Recalled by Baxter Healthcare...

The Issue: Inadequate iodine and packaging related defects.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo¿ Advanced Perfusion System 1 100/120V AC Recalled by Terumo...

The Issue: An evaluation of the APS1 Operator Manual found that existing instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2014· Nidek Inc

Recalled Item: Non-Mydriatic Auto Fundus Camera. Model AFC-330. An ophthalmic camera for...

The Issue: Image taken by AFC-330 has a white spot which may affect diagnosis or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2014· McKesson Technologies, Inc.

Recalled Item: Paragon Laboratory Management Recalled by McKesson Technologies, Inc. Due to...

The Issue: For Paragon Laboratory Management 12.1 and 12.1.1 releases, if used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2014· Philips Medical Systems, Inc.

Recalled Item: Ingenia 3.0T Recalled by Philips Medical Systems, Inc. Due to For some...

The Issue: For some identified Ingenia systems shipped between December 2013 and March...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2014· Philips Medical Systems, Inc.

Recalled Item: Ingenia 1.5T R5 Recalled by Philips Medical Systems, Inc. Due to For some...

The Issue: For some identified Ingenia systems shipped between December 2013 and March...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2014· Philips Medical Systems, Inc.

Recalled Item: Ingenia 3.0T R5 Recalled by Philips Medical Systems, Inc. Due to For some...

The Issue: For some identified Ingenia systems shipped between December 2013 and March...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Partial loss of...

The Issue: Partial loss of monitoring with the CARESCAPE Monitor B850, B650 or B450....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2014· Philips Medical Systems, Inc.

Recalled Item: Ingenia 1.5T Recalled by Philips Medical Systems, Inc. Due to For some...

The Issue: For some identified Ingenia systems shipped between December 2013 and March...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Zimmer Manufacturing B.V.

Recalled Item: Zimmer EDI PERIARTICULAR PLATING SYSTEM CANCELLOUS BONE SCREW Recalled by...

The Issue: Two lots of screws were commingled. Screws with etching and machining for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Heartsine Technologies, Limited

Recalled Item: Pad-Pak and Pedi-Pak accessories for the HeartSine Samaritan PAD 300P...

The Issue: A small number of sealed foil pouches containing the electrodes were found...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Biolase Technology Inc

Recalled Item: WaterLase iPlus Dental Laser System Recalled by Biolase Technology Inc Due...

The Issue: Biolase is recalling the WaterLase iPlus Dental Laser System because of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2014· Pentax Medical Company

Recalled Item: EG-3630U Ultrasound Video Gastroscope EG-3830UT Ultrasound Video Gastroscope...

The Issue: Aspiration needles used in combination with Ultrasound Gastroscopes can...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2014· Integra LifeSciences Corp.

Recalled Item: Integra¿ LED Battery Charger Recalled by Integra LifeSciences Corp. Due to...

The Issue: LED battery chargers may prematurely fail and will not charge the LED...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2014· PIONEER SURGICAL TECHNOLOGY, INC.

Recalled Item: Tritium Sternal Plate System Recalled by PIONEER SURGICAL TECHNOLOGY, INC....

The Issue: Lack of Sterility Assurance

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2014· GE Healthcare, LLC

Recalled Item: DATEX-OHMEDA S/5 SINGLE-WIDTH AIRWAY MODULE Recalled by GE Healthcare, LLC...

The Issue: Failure of the CO2 detector in Single-width Airway and Extension modules,...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 11, 2014· Hitachi Aloka Medical, Ltd.

Recalled Item: Prosound F75 or F75 The Hitachi Aloka Medical Recalled by Hitachi Aloka...

The Issue: Loosened monitor arm.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2014· Baxter Healthcare Corp.

Recalled Item: EXACTAMIX 1200 Compounder Recalled by Baxter Healthcare Corp. Due to If the...

The Issue: If the universal ingredient (UI) in an active configuration is changed using...

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

Class II — Potential Health HazardOngoing