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. 2,632 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,632 in last 12 months

Showing 3366133680 of 53,621 recalls

DrugJanuary 5, 2017· Sun Pharmaceutical Industries, Inc.

Recalled Item: Alfuzosin Hydrochloride Extended-release Tablets Recalled by Sun...

The Issue: Presence of Foreign Substance: consumer complaint for foreign matter...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 5, 2017· Haag-Streit USA Inc

Recalled Item: EyeSuite i.8.2.1.0 Software for ophthalmic use including selection of Intra...

The Issue: There is a possibility for data to be stored under the wrong patient on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2017· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products FS Calibrator 1 Recalled by Ortho-Clinical...

The Issue: The company received a customer complaint for the inability to calibrate...

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

Class III — Low RiskOngoing
FoodJanuary 4, 2017· Dutch Valley Food Distributors Inc.

Recalled Item: Cappuccino Snack Mix Lot code: 20161027 Recalled by Dutch Valley Food...

The Issue: As a result of an ingredient supplier recall, Dutch Valley is issuing a...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 4, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: IMMULITE 2000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc...

The Issue: DHEA-S causes falsely elevated progesterone results.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: IMMULITE/ IMMULITE 1000 Progesterone Recalled by Siemens Healthcare...

The Issue: DHEA-S causes falsely elevated progesterone results.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Dimension Vista LOCI Progesterone Recalled by Siemens Healthcare...

The Issue: DHEA-S causes falsely elevated progesterone results.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Progesterone Recalled by Siemens Healthcare Diagnostics, Inc...

The Issue: DHEA-S causes falsely elevated progesterone results.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2017· Zimmer Biomet, Inc.

Recalled Item: Vanguard Total Knee System Vanguard Open Box Femoral Components Item...

The Issue: packaging of some femoral components was incorrectly labeled as either...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2017· Baxter Healthcare Corporation

Recalled Item: Maintenance Kit PH2 Recalled by Baxter Healthcare Corporation Due to Baxter...

The Issue: Baxter Healthcare Corporation is issuing a voluntary product recall for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2017· Baxter Healthcare Corporation

Recalled Item: Maintenance Kit PH1 Recalled by Baxter Healthcare Corporation Due to Baxter...

The Issue: Baxter Healthcare Corporation is issuing a voluntary product recall for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2017· Endologix

Recalled Item: AFX2 Endovascular AAA System Item No. Item Description F00820-01...

The Issue: Endologix updated information on the rates of Type III endoleaks and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2017· Endologix

Recalled Item: AFX Endovascular AAA System Item Number Item Description F0070305 A2525/C75...

The Issue: Endologix updated information on the rates of Type III endoleaks and...

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

Class II — Potential Health HazardOngoing
FoodJanuary 3, 2017· Del Dee Foods Inc.

Recalled Item: Hemp & Grain Co. Recalled by Del Dee Foods Inc. Due to Potential Salmonella...

The Issue: Del Dee Foods, Inc.withdrew Lot# PP33116-0-D after receiving a report of...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 3, 2017· High Liner Foods, Inc.

Recalled Item: FPI Breaded Round Shrimp Tail-On 1001990 Recalled by High Liner Foods, Inc....

The Issue: Product contains undeclared milk and eggs

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 3, 2017· Stryker Leibinger GmbH & Co. KG

Recalled Item: 9805 Orbital Volume Sizer Set with Tray (Non-sterile) 9951 Design Recalled...

The Issue: An incorrect sterility status on the label, non-sterile products labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2017· Stryker Leibinger GmbH & Co. KG

Recalled Item: QUINTUBE Monitor Pack (5 tubes/pk Recalled by Stryker Leibinger GmbH & Co....

The Issue: An incorrect sterility status on the label, non-sterile products labeled as...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 1, 2017· BioMerieux SA

Recalled Item: Ceftriaxone TX 32 US S30 Recalled by BioMerieux SA Due to Potential...

The Issue: Potential performance issue on strain categorization.

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

Class II — Potential Health HazardOngoing
FoodDecember 30, 2016· Blommer Chocolate Co., Inc.

Recalled Item: Butterscotch Drops - MB 1000 [or 4000] Count Recalled by Blommer Chocolate...

The Issue: Possible contamination of product with Salmonella as product includes the...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 30, 2016· Blommer Chocolate Co., Inc.

Recalled Item: 70 Milk Confectionery Coating - MB Recalled by Blommer Chocolate Co., Inc....

The Issue: Possible contamination of product with Salmonella as product includes the...

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

Class I — Serious Health HazardOngoing
Refund