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 2238122400 of 28,172 recalls

Medical DeviceApril 1, 2015· Viewray Incorporated

Recalled Item: Patient Handling System (Motion Control Software) Recalled by Viewray...

The Issue: ViewRay received a report that the couch moved unexpectedly into the bore...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2015· Dako North America Inc.

Recalled Item: Test Request Distributor (TRD 1.3 and TRD 1.4) Recalled by Dako North...

The Issue: If a user requests slides from the LIS or TPID, then updates a request by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2015· Teleflex Medical

Recalled Item: Teleflex Medical Hudson RCI ConchaTherm Neptune Heated Humidifier Recalled...

The Issue: Customer complaints were received of power to the unit ceasing and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2015· VasoNova, Inc.

Recalled Item: VasoNova Vascular Positioning System (VPS ) G4 Console Catalog number...

The Issue: A limited number of VPS G4 Consoles are being recalled due to noncompliance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2015· OriGen Biomedical, Inc.

Recalled Item: OriGen BIOMEDICAL VV13F Reinforced Dual Lumen Catheter STERILE DISPOSABLE:...

The Issue: Potential for clear extension tube to separate from the hub, which could...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 30, 2015· Baylis Medical Corp *

Recalled Item: ProTrack Microcatheter Recalled by Baylis Medical Corp * Due to Baylis...

The Issue: Baylis Medical Company is recalling two lots of ProTrack Microcatheter due...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2015· Integra LifeSciences Corp. d.b.a. Integra Pain Management

Recalled Item: Integra Long Epidural Steroid Injection Needle (Tuohy Needle) Recalled by...

The Issue: A single lot of 18 Gauge, 3.5 inch Tuohy Needles were incorrectly packaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2015· OriGen Biomedical, Inc.

Recalled Item: Reinforced Dual Lumen Cannula Recalled by OriGen Biomedical, Inc. Due to...

The Issue: Potential for clear extension tube to separate from the hub, which could...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 27, 2015· B. Braun Medical, Inc.

Recalled Item: CONTIPLEX Continuous Peripheral Nerve Block Tray Recalled by B. Braun...

The Issue: There is a potential for a hole to be present in the outer tray of a limited...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2015· Amtryke LLC

Recalled Item: AmTryke Model 1424 Community Cruiser Hand Cycle. Therapeutic tricycle....

The Issue: Product is being recalled due to complaints of cracked frames.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2015· Becton Dickinson & Co.

Recalled Item: BBL Trypticase Soy Agar with 5% Sheep Blood (TSA II) Recalled by Becton...

The Issue: BD has confirmed that one lot of TSA II and Chocolate Agar I-Plates may fail...

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

Class III — Low RiskOngoing
Medical DeviceMarch 26, 2015· Olympus America Inc.

Recalled Item: EVIS EXERA II Duodenovideoscope OLYMPUS TJF TypeQ180V. This instrument has...

The Issue: New and validated reprocessing procedures have been issued for the Olympus...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 1/4 in. Trocar with Single Drain Curved Trocar with Wound Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 1/4 in. Round Drain with Trocar Curved Trocar with Wound Recalled by Stryker...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 3/16 in. Curved Trocar with Wound Drain Curved Trocar with Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 3/16 in. Double Trocar with Wound Drain Curved Trocar with Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· PhotoMedex, Inc.

Recalled Item: Iamin Moist Dressing and the Iamin Hydrating Gel: intended to Recalled by...

The Issue: The labeling for the Iamin family of medical devices (e.g. printed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 1/8 in. Curved Trocar with Wound Drain Curved Trocar with Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 1/8 in. Double Trocar with Wound Drain Curved Trocar with Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 1/4 in. Double Trocar with Wound Drain Curved Trocar with Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...

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

Class II — Potential Health HazardOngoing