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.
Showing 34021–34040 of 53,621 recalls
Recalled Item: Toms of Maine Naturally Dry Natural Powder Antiperspirant Stick Recalled by...
The Issue: Labeling: Label Mix Up- Incorrect back label applied to the product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: WHITE BEAN Recalled by Hale And Hearty Soups, LLC Due to Potential Listeria...
The Issue: Potential contamination with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MULLIGATAWNY Recalled by Hale And Hearty Soups, LLC Due to Potential...
The Issue: Potential contamination with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Plush Puffs Marshmallows Toasty Coconut 4oz. and 2lb bulk bag Recalled by To...
The Issue: Undeclared allergen of milk from the declared ingredient coconut cream powder.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Durex Pleasure Pack . 3 ultra fine lubricated latex condoms Recalled by...
The Issue: Reckitt Benckiser LLC is recalling Durex Condoms Pleasure Packs due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS IMMULITE 2000/2000 Xpi Systems Intact PTH (Parathyroid Hormone) Test...
The Issue: Siemens is conducting this recall for the IMMULITE¿ 2000/IMMULITE¿ 2000 XPi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G3 Opticage Expandable Interbody Fusion Device Recalled by Interventional...
The Issue: During implantation, the proximal end of the device could separate if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire 1.4mm x 12in Non-Threaded Recalled by Amendia, Inc Due to The rods...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Widow 6.6mm x 20mm Screw Recalled by Amendia, Inc Due to There is a...
The Issue: There is a problem with the mating feature between the plate and screw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Stylet Needle Recalled by Amendia, Inc Due to The rods are packaged in...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Savannah-T Straight Rod Recalled by Amendia, Inc Due to The rods are...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Recalled by Teleflex Medical Due to Labeling Inconsistency: The...
The Issue: Labeling Inconsistency: The products have been labeled with the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Widow Plate 19mm Plate Recalled by Amendia, Inc Due to There is a...
The Issue: There is a problem with the mating feature between the plate and screw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyberKnife Robotic Radiosurgery System using software version 10.6 Recalled...
The Issue: Accuray has become aware of a potential safety issue involving unexpected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mallinckrodt Pharmaceuticals INOmax DSIR Plus delivery system. Model 10007....
The Issue: Mallinckrodt discovered that some devices may have been manufactured with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GalaSHAPE 3D Recalled by Tepha Incorporated Due to Endotoxin values from...
The Issue: Endotoxin values from testing of retains slightly exceeded the established...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prestige VH Recalled by GE Healthcare, LLC Due to GE Healthcare is...
The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precision 500D Recalled by GE Healthcare, LLC Due to GE Healthcare is...
The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTX LCA Recalled by GE Healthcare, LLC Due to GE Healthcare is...
The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prestige SI Recalled by GE Healthcare, LLC Due to GE Healthcare is...
The Issue: GE Healthcare is conducting a recall due to the potential fall of aged CRT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.