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. 2,639 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,639 in last 12 months

Showing 3288132900 of 53,621 recalls

DrugMarch 10, 2017· Claris Lifesciences Inc

Recalled Item: Fluconazole Injection Recalled by Claris Lifesciences Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2017· Claris Lifesciences Inc

Recalled Item: Levofloxacin Injection in 5% Dextrose Recalled by Claris Lifesciences Inc...

The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2017· Claris Lifesciences Inc

Recalled Item: Ciprofloxacin in Dextrose (5%) Injection Recalled by Claris Lifesciences Inc...

The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 10, 2017· Claris Lifesciences Inc

Recalled Item: Metronidazole Injection Recalled by Claris Lifesciences Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility: there is potential of a leak from the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 10, 2017· Nestle USA

Recalled Item: Haagen-Dazs Chocolate Dark Chocolate Ice Cream Bars Recalled by Nestle USA...

The Issue: Firm received two complaints of finding a Haagen-Dazs Vanilla Milk Almond...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
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· 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· 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: 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· Cincinnati Sub-Zero Products Inc

Recalled Item: Hemotherm CE Recalled by Cincinnati Sub-Zero Products Inc Due to Improperly...

The Issue: Improperly rated fuses were used in the manufacture of the device.

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· 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
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· 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: 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: 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: 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: 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