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. 2,551 recalls have been distributed to New Jersey in the last 12 months.
Showing 46501–46520 of 53,621 recalls
Recalled Item: GemStar Docking Station Recalled by Hospira Inc. Due to There are two...
The Issue: There are two situations that may occur when using the GemStar Docking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Newman's Own Salsa Con Queso Recalled by Newman'S Own Inc. Due to Undeclared...
The Issue: Undeclared wheat
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Triton FP Infusion Pump Recalled by WalkMed Infusion, LLC Due to WalkMed...
The Issue: WalkMed Infusion is initiaing a recall on their Triton FP Infusion Pump,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XiO RPT System The XiO RTP System is used to Recalled by Elekta, Inc. Due to...
The Issue: Dose and Monitor Unit values are not computed correctly when Elekta...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Healthcare G2 Clinical Access Mislabeled CDs for PN: 063-1829-11...
The Issue: Spacelabs has voluntarily recalled G2 Clinical Access Software CD because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT580/Discovery CT590RT scanners running software...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL Recalled by Philips Medical Systems, Inc. Due to...
The Issue: Philips HeartStart XL may experience a power board failure causing failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Device Name: ABX PENTRA ML Model/Part #(s): A11A01652 Lot/Serial #(s):...
The Issue: HORIBA Medical initiated this recall of all software versions of ABX PENTRA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RaySearch Ray Station Radiation Therapy Treatment Planning System Recalled...
The Issue: RaySearch Laboratories has recalled "RaySearch Ray Station 2.0, 2.5, 3.0,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acetylcysteine Solution Recalled by Ben Venue Laboratories Inc Due to...
The Issue: Presence of Particulate Matter: During a review of retain samples, the firm...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CITRULLINE (L) in 25 g Recalled by Medisca Inc Due to Labeling: Label...
The Issue: Labeling: Label Mix-Up: FDA tested samples of API from Medisca, labeled as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Capsules Recalled by Legacy Pharmaceutical Packaging Due to...
The Issue: Chemical Contamination: The recalling firm received notice that their...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: etomidate injection Recalled by Agila Specialties Private Ltd. Due to...
The Issue: Presence of Particulate Matter: Potential for small black particles to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE Healthcare Solar 8000M and Solar 8000i Patient Monitor software version...
The Issue: GE Healthcare has recently become aware of a potential safety issue with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerifyNow IIb/IIIa Test Recalled by Accumetrics Inc Due to Accumetrics is...
The Issue: Accumetrics is recalling the VerifyNow IIb/IIIa test because it may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Other Macaroon G'nache P'nache 5.3 oz. Manufactured and Distributed...
The Issue: Northern Valley Baking Company did not declare milk or soy on the allergen...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CartoUnivu Module Recalled by Biosense Webster, Inc. Due to Biosense Webster...
The Issue: Biosense Webster has initiated a recall of the CartoUnivu Module within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT Intact PTH Controls consists of 3 x 1 Bottle Recalled by Abbott...
The Issue: Abbott has confirmed that a performance shift in the ARCHITECT Intact PTH...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.