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. 2,616 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,616 in last 12 months

Showing 3742137440 of 53,621 recalls

Medical DeviceMarch 10, 2016· Ferno-Washington Inc

Recalled Item: Poly-bags containing the strap labeled with "Adult" sticker. Each strap...

The Issue: On March 9, 2016, the firm was contacted regarding the possibility of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 10, 2016· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius 2008 Series Hemodialysis Delivery Systems: 2008T Recalled by...

The Issue: Added Warning Statement: Fresenius 2008 Series Hemodialysis Machines False...

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

Class II — Potential Health HazardOngoing
DrugMarch 9, 2016· Teva Pharmaceuticals USA

Recalled Item: Amikacin Sulfate injection USP Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Presence of Particulate Matter: particulate matter identified as glass in...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 9, 2016· Whole Foods Market

Recalled Item: 365 Everyday Value Mango Frozen Fruit Bars 4 Bars-4 fl. Recalled by Whole...

The Issue: Undeclared coconut

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 9, 2016· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Panorama Patient Monitoring Network Mindray DS USA The Panorama Patient...

The Issue: Panorama Central Station including the work station View Station, View...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2016· Biomet, Inc.

Recalled Item: All instrumentation associated with the Prelude PF Resurfacing Knee System....

The Issue: Inadequate design control.

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

Class II — Potential Health HazardOngoing
DrugMarch 8, 2016· Hospira Inc.

Recalled Item: Dextrose Injection Recalled by Hospira Inc. Due to Chemical Contamination:...

The Issue: Chemical Contamination: Potential for contamination of the products with an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 8, 2016· Hospira Inc.

Recalled Item: Mannitol I.V. Recalled by Hospira Inc. Due to Chemical Contamination:...

The Issue: Chemical Contamination: Potential for contamination of the products with an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 8, 2016· Hospira Inc.

Recalled Item: Dextrose Injection Recalled by Hospira Inc. Due to Chemical Contamination:...

The Issue: Chemical Contamination: Potential for contamination of the products with an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 8, 2016· Hospira Inc.

Recalled Item: Dextrose Injection Recalled by Hospira Inc. Due to Chemical Contamination:...

The Issue: Chemical Contamination: Potential for contamination of the products with an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 8, 2016· Hospira Inc.

Recalled Item: Potassium Chloride Injection 20 mEq Recalled by Hospira Inc. Due to Chemical...

The Issue: Chemical Contamination: Potential for contamination of the products with an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 8, 2016· Hospira Inc.

Recalled Item: Aminosyn-PF (amino acids) 7% Recalled by Hospira Inc. Due to Chemical...

The Issue: Chemical Contamination: Potential for contamination of the products with an...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 8, 2016· Welle Pty Ltd

Recalled Item: The Super Elixir By WelleCo Australia Alkalising Greens 150g/5.3 oz net...

The Issue: Welle Pty Ltd is recalling Wellco Super Elixir pouches because of potential...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 8, 2016· Hill-Rom, Inc.

Recalled Item: Liko Universal SlingBars Universal SlingBar" 350 Recalled by Hill-Rom, Inc....

The Issue: The center bolt of the sling bar, which connects the bar to the patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Syva Emit Methotrexate Assay Recalled by Siemens Healthcare Diagnostics,...

The Issue: Siemens Healthcare Diagnostics confirmed that Syva Emit Methotrexate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2016· ICU Medical, Inc.

Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...

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

Class II — Potential Health HazardOngoing