Product Recalls in New Jersey

Product recalls affecting New Jersey — including food, drugs, consumer products, medical devices, and vehicles distributed to New Jersey. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,642 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,642 in last 12 months

Showing 2820128220 of 29,496 recalls

Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Superstat Corp

Recalled Item: Superstat Modified Collagen Hemostatic Sponge Recalled by Superstat Corp Due...

The Issue: The recall was initiated because Superstat Corporation has confirmed that no...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2012· Nidek Inc

Recalled Item: Nidek MC-500 Multicolor Laser Photocoagulator using software version 2.20....

The Issue: When the MC-500 is turned on and coagulation is performed without changing...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2012· Siemens Medical Solutions USA, Inc.

Recalled Item: The Siemens Symbia T series is intended to aid in detecting Recalled by...

The Issue: There is a potential for the linear bearing car to fail allowing the ball...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2012· Siemens Medical Solutions USA, Inc.

Recalled Item: The Siemens Symbia S series is intended to aid in detecting Recalled by...

The Issue: There is a potential for the linear bearing car to fail allowing the ball...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Accolade TMZF Plus 127 degree Neck Angle V40 Hip Stem Recalled by Stryker...

The Issue: Stryker has received a report that single size 3.5 stem was packaged as size...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2012· Becton Dickinson & Co.

Recalled Item: BD BBL Taxo XV Factor Strips Recalled by Becton Dickinson & Co. Due to In...

The Issue: In vitro diagnostic test kit was not manufactured according to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2012· Alere San Diego, Inc.

Recalled Item: Alere Cholestech LDX Calibration Verification Recalled by Alere San Diego,...

The Issue: Out of range (increased) HDL Cholesterol results.

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

Class III — Low RiskOngoing
Medical DeviceOctober 22, 2012· Alere San Diego, Inc.

Recalled Item: Alere Cholestech LDX Multianalyte Control Recalled by Alere San Diego, Inc....

The Issue: Out of range (increased) HDL Cholesterol results.

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

Class III — Low RiskOngoing
Medical DeviceOctober 19, 2012· TITAN SPINE, LLC

Recalled Item: Titan Spine Endoskeleton TA Implant products. 2107-0118 18mm Standard...

The Issue: Titan Spine LLC, is conducting a recall on the Endoskeleton TA VBR products....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2012· Trivascular, Inc

Recalled Item: TriVascular brand Fill Polymer Kit Recalled by Trivascular, Inc Due to...

The Issue: Selected lots of the Fill Polymer Kit (European Model Number: TVFP14- B) in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2012· American Medical Systems, Inc.

Recalled Item: AMS AdVance" Male Sling System 720088-01 AMS AdVance" Male Sling Recalled by...

The Issue: American Medical Systems¿ (AMS) is issuing a voluntary recall on a number of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2012· Innovative Magnetic Resonance Imaging Systems Inc.

Recalled Item: IMRIS ORT100 (Part Number 110470-000) and ORT200 (Part Number 112216-00)...

The Issue: IMRIS Inc. initiated a recall of their OR Tables ORT100 and ORT200. When...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2012· Philips And Neusoft Medical Systems Co., Ltd.

Recalled Item: NeuViz 16 Multi-Sliced CT Scanner System Recalled by Philips And Neusoft...

The Issue: The four screws that secure the patient table top to the carrier pulled out...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2012· OrthoPediatrics Corp

Recalled Item: 4.5mm PLEO Osteotomy Guide. OrthoPediatrics Corp. markets a pediatric...

The Issue: Complaint received from sales representative that the drill guide tubes...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2012· Biomerieux Inc

Recalled Item: 0.9% Sodium Chloride Injections Recalled by Biomerieux Inc Due to The firm...

The Issue: The firm inventoried and distributed 0.9% Sodium Chloride Saline bags as...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: HX2 Temp Manage SYS 120V The Terumo HX2 Temperature Management Recalled by...

The Issue: Based on a retrospective review of quality data, AC Control boards used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Tested AC Control BD Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Based on a retrospective review of quality data, AC Control boards used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Vital Signs Devices, a GE Healthcare Company

Recalled Item: Corometrics Qwik Connect Plus Spiral Electrode- Model #7000AA0 A fetal...

The Issue: Thirty fetal scalp electrodes were found to have an incomplete package seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2012· Toshiba American Medical Systems Inc

Recalled Item: MRT-1504/A4 - Titan X MRI System MRT-30 I0A/5 - Titan Recalled by Toshiba...

The Issue: It was found that there is a problem with the LCD monitor used in the...

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

Class II — Potential Health HazardOngoing