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. 2,729 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,729 in last 12 months

Showing 1912119140 of 29,496 recalls

Medical DeviceMarch 14, 2017· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Connect Diabetes Management App versions 2.0.0 Recalled by Roche...

The Issue: A program error (bug) in the Bolus Advisor feature, which could result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2017· Instradent USA, Inc.

Recalled Item: NEODENT CM Intraoral Scanbody Recalled by Instradent USA, Inc. Due to During...

The Issue: During internal testing, Neodent determined that the body diameter (3.8mm)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2017· Valeant Pharmacueticals International

Recalled Item: Small Particle Aerosol Generator Model SPAG-2 6000 Series (SPAG-2). The...

The Issue: SPAG-2 unit nebulizers from Lot J0571670RA were tested at Next Breath for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2017· Measurement Specialties Inc

Recalled Item: Measurement Specialties Reusable Temperature Probe Autoclavable. Sold as...

The Issue: The reusable temperature probes are provided with instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2017· Nihon Kohden America Inc

Recalled Item: Bedside monitor CSM-1901(Life Scope G9) with main unit CU-192RA. The...

The Issue: The Pause function on central monitors will not automatically resume when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2017· Accelerate Diagnostics Inc

Recalled Item: Accelerate Pheno system Recalled by Accelerate Diagnostics Inc Due to Rare...

The Issue: Rare isolates of Enterobacteriaceae may generate a susceptible meropenem...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2017· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is...

The Issue: Product shipped proximate to or past the expiration date listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2017· Heartware

Recalled Item: HeartWare Ventricular Assist System (HVAD) Pump Driveline Splice Kit Product...

The Issue: In April 2015, HeartWare, now a part of Medtronic, notified users of a...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 9, 2017· Smith & Nephew, Inc.

Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...

The Issue: The expiration dates on the labeling are incorrect, the actual expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· C.R. Bard, Inc.

Recalled Item: SURESTEP Tray Recalled by C.R. Bard, Inc. Due to Misbranded: Product...

The Issue: Misbranded: Product labeled, Not made with natural rubber latex, may in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Centurion Medical Products Corporation

Recalled Item: OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye Pads are Recalled by...

The Issue: Centurion Medical Products is recalling Convenience Kits that contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Centurion Medical Products Corporation

Recalled Item: POST-OPERATIVE OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye Pads...

The Issue: Centurion Medical Products is recalling Convenience Kits that contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Centurion Medical Products Corporation

Recalled Item: POST-OP EYE TRAY The Covidien Curity Oval Eye Pads are Recalled by Centurion...

The Issue: Centurion Medical Products is recalling Convenience Kits that contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Centurion Medical Products Corporation

Recalled Item: OPHTHALMIC DRS TRAY The Covidien Curity Oval Eye Pads are Recalled by...

The Issue: Centurion Medical Products is recalling Convenience Kits that contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Centurion Medical Products Corporation

Recalled Item: OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye Pads are Recalled by...

The Issue: Centurion Medical Products is recalling Convenience Kits that contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Centurion Medical Products Corporation

Recalled Item: EYE KIT The Covidien Curity Oval Eye Pads are individually Recalled by...

The Issue: Centurion Medical Products is recalling Convenience Kits that contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Centurion Medical Products Corporation

Recalled Item: CUSTOM CADAVER KIT The Covidien Curity Oval Eye Pads are Recalled by...

The Issue: Centurion Medical Products is recalling Convenience Kits that contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Smith & Nephew, Inc.

Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...

The Issue: The expiration dates on the labeling are incorrect, the actual expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Smith & Nephew, Inc.

Recalled Item: Peri-Loc(R) VLP 3.5 MM X 6 MM SELF-TAPPING CORTEX SCREW Recalled by Smith &...

The Issue: The expiration dates on the labeling are incorrect, the actual expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Keystone Dental Inc

Recalled Item: Keystone Dental Inc. PrimaConnex Straight Implant TC Recalled by Keystone...

The Issue: Straight PrimaConnex Implants contained Tapered PrimaConnex Implants

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

Class II — Potential Health HazardOngoing