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. 2,603 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,603 in last 12 months

Showing 4038140400 of 53,621 recalls

DrugJuly 2, 2015· Bestco, Inc.

Recalled Item: CVS SUGAR FREE BLACK CHERRY COUGH DROPS (MENTHOL-COUGH SUPPRESSANT) Recalled...

The Issue: Presence of Foreign Tablets/Capsules: Presence of comingled Sugar Free Honey...

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

Class III — Low RiskOngoing
Refund
FoodJuly 2, 2015· Barilla America NY, Inc.

Recalled Item: Barilla MEDIUM SHELLS Recalled by Barilla America NY, Inc. Due to Barilla...

The Issue: Barilla America NY, Inc. has recalled four types of pasta due to the...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 2, 2015· Barilla America NY, Inc.

Recalled Item: Barilla Packaged Specifically for FoodService Recalled by Barilla America...

The Issue: Barilla America NY, Inc. has recalled four types of pasta due to the...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 2, 2015· Barilla America NY, Inc.

Recalled Item: Barilla PENNE Recalled by Barilla America NY, Inc. Due to Barilla America...

The Issue: Barilla America NY, Inc. has recalled four types of pasta due to the...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 2, 2015· Barilla America NY, Inc.

Recalled Item: Barilla Pronto PENNE Recalled by Barilla America NY, Inc. Due to Barilla...

The Issue: Barilla America NY, Inc. has recalled four types of pasta due to the...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 2, 2015· Arthur Schuman Inc.

Recalled Item: Bella Rosa Parmesan Net Wt. 20 oz (567 g) 1.25 LB Arthur Schuman Recalled by...

The Issue: Bella Rosa Grated Parmesan Cheese may contain undeclared egg lysozyme.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 2, 2015· Stryker Medical Division of Stryker Corporation

Recalled Item: Spirit One A-C Powered Hospital Bed Recalled by Stryker Medical Division of...

The Issue: Inaccurate scale systems

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2015· Stryker Medical Division of Stryker Corporation

Recalled Item: Spirit One A-C Powered Hospital Bed Recalled by Stryker Medical Division of...

The Issue: Customer complaints associated with faulty brake system

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2015· Cook Inc.

Recalled Item: Beacon Tip Royal Flush Plus High-Flow Catheter. Angiographic catheter. For...

The Issue: Reports of catheter tip splits and or separation. Loss of device function,...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 2, 2015· Cook Inc.

Recalled Item: Slip-Cath Beacon Tip Catheter. Angiographic catheter. For use in...

The Issue: Reports of catheter tip splits and or separation. Loss of device function,...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 2, 2015· Cook Inc.

Recalled Item: Beacon Tip Torcon NB Advantage Catheter. Angiographic catheter. For use...

The Issue: Reports of catheter tip splits and or separation. Loss of device function,...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF Big Bore CT/PET System. The Philips GEMINI PET/CT Recalled by...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF 16 Slice CT/PET System. The Philips GEMINI PET/CT Recalled by...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI GXL 16 Slice CT/PET System. The Philips GEMINI PET/CT Recalled by...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Myoscience Inc

Recalled Item: iovera 155 Smart Tip Recalled by Myoscience Inc Due to The expiration date...

The Issue: The expiration date on the outer box label and the pouch label for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF 64 Slice CT/PET System. The Philips GEMINI PET/CT Recalled by...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF Ready CT/PET System. The Philips GEMINI PET/CT Imaging Recalled by...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI LXL CT/PET System. The Philips GEMINI PET/CT Imaging Systems Recalled...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF Base CT/PET System. The Philips GEMINI PET/CT Imaging Recalled by...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Elekta, Inc.

Recalled Item: MOSAIQ Oncology Information System MOSAIQ is an oncology information system...

The Issue: A problem exists in MOSAIQ resulting in the incorrect field size being sent...

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

Class II — Potential Health HazardOngoing