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. 2,683 recalls have been distributed to New Jersey in the last 12 months.
Showing 22761–22780 of 53,621 recalls
Recalled Item: CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM - Product Usage: Instrument intended...
The Issue: possibility of the sterility batch being insufficiently sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Swivel Elbow with Bronchoscopy Port 15MM OD Recalled by Intersurgical...
The Issue: The port may crack in the swivel elbow where the flip cap is inserted, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIMAN DISP.INSTR.ARTICULAT.D:12/440MM Product Usage: Instrument intended...
The Issue: possibility of the sterility batch being insufficiently sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Recalled by...
The Issue: Products may contain the incorrect banner card within the kit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASI 2.0 Calcar Trimmer Shaft for Use with Biomet¿ Rasp Recalled by Zimmer...
The Issue: The potential that the end of the shaft could fail to effectively mate with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8.5 Fr. X 10 cm ARROW+gard Blue PSI Kit Cath-Gard Recalled by Arrow...
The Issue: Products may contain the incorrect banner card within the kit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amy's Bowls - Broccoli & Cheddar Bake Recalled by Amys Kitchen Inc Due to...
The Issue: Consumer complaints of black plastic found in product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Short Fill: fill...
The Issue: Short Fill: fill volume was out of specification at 94 mL (specification: no...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS) for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS) for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BodyGuardian Heart Remote Monitoring Kit Recalled by Preventice Services,...
The Issue: The device data being collected and transferred to the monitoring center may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PreGel Lemon 50 4.4 lb (2kg) bag Recalled by PreGel America, Inc. Due to...
The Issue: Undeclared Milk. The firm received a complaint that there was milk in the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Entenmann's Little Bites Soft Baked Cookies (5 pack Mini Chocolate Recalled...
The Issue: Possible presence of small plastic pieces caused by a manufacturing failure.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel Recalled...
The Issue: The mounts on the monitor may have an insufficient weld.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rocket KCH Fetal Bladder Drainage Catheter Model: R57405 Recalled by Rocket...
The Issue: A complaint was received regarding kinking of the device prior to use. If a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LightPod Neo Lasers Recalled by Aerolase Corporation Due to This relates to...
The Issue: This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gold Cup Leadwire and Snap Leadwire with the following component Recalled by...
The Issue: The electrode lead connector has a protruding conductor beyond insulation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LightPod ERA lasers Recalled by Aerolase Corporation Due to This relates to...
The Issue: This relates to the standard 21 CFR 1040.10(f)(3) requiring a readily...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Up Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM go.Top Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The injector holder could potentially fall off together with the injector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.