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.
Showing 36661–36680 of 53,621 recalls
Recalled Item: Ingenuity Core Model No. 728321 Recalled by Philips Medical Systems...
The Issue: Software issues in software versions v4.1.3/4.1.4/4.1.5 in the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT Model No. 728326 Recalled by Philips Medical Systems...
The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: Software issues in versions v4.1 .3/4.1.5 in the Philips Brilliance iCT) iCT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core128 Model No. 728323 Recalled by Philips Medical Systems...
The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sclerosol Intrapleural Aerosol (sterile talc powder) Recalled by Lymol...
The Issue: Defective Delivery System: Defective stem valve causes leakage of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zoloft (sertraline HCl) tablets Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: thick tablets exceeding specifications...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IMPAK ELASTIC ACRYLIC RESIN POWDER & LIQUID Recalled by CMP Industries, Llc...
The Issue: Possible presence of foreign material (rust).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAK Liquid Acrylic Resin sold under the following labels: 1) Recalled by...
The Issue: Possible presence of foreign material (rust).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Excelsior Disposable Syringe Heparin Lock Flush Recalled by Excelsior...
The Issue: Certain lots of Heparin Lock Flush, USP Syringes (5 ml Fill in 10 ml...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hectorol (doxercalciferol injection) 2 mcg/1mL Recalled by Genzyme...
The Issue: Labeling: Wrong barcode. An incorrect bar code was noted on the vial label...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norditropin FlexPro Somatropin (rDNA origin) injection Recalled by Novo...
The Issue: Defective Delivery System; may have a low frequency assembly fault which may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Linezolid Injection Recalled by Teva North America Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility: Due to potential for leaking bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mighty Leaf Tea Company Organic Ginger Peach Iced Tea Recalled by Mighty...
The Issue: Firm was notified by their supplier of Organic Ginger Peach tea that it has...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Firebird NXG Spinal Fixation System Set Screw Driver used to Recalled by...
The Issue: There is a possibility that the subject set screw driver could disengage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4 ml FX Sodium Fluoride/Potassium Oxalate tube Recalled by Greiner Bio-One...
The Issue: The 4 ml FX Sodium Fluoride/Potassium Oxalate tube may have no or low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Microline Scissor Tips intended to be used with a Recalled by...
The Issue: Sterlilmed is recalling all unexpired Scissor Tips because of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WHIN Infusion Set - 90 Huber Needle and Wing (22 Recalled by B. Braun...
The Issue: Potential for the tip of the Huber needle on the WHIN Infusion Set to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensorcaine- MPF (Bupivacaine HCI Injection Recalled by Fresenius Kabi USA,...
The Issue: Presence of Particulate Matter: Glass particulate found in sterile...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Toshiba America Medical Systems Recalled by Toshiba American Medical Systems...
The Issue: It has been found that if the scan range extends beyond the maximum Field of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba America Medical Systems Recalled by Toshiba American Medical Systems...
The Issue: It has been found that if the scan range extends beyond the maximum Field of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.