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. 2,743 recalls have been distributed to New Jersey in the last 12 months.
Showing 17841–17860 of 29,496 recalls
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...
The Issue: The barcode label was placed underneath the sterile barrier and the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OneStep CPR Complete Recalled by ZOLL Medical Corporation Due to A portion...
The Issue: A portion of one lot of ZOLL OneStep Complete Electrodes for adults will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Response 5.5/6.0 Spine System 7.0mm x 40mm Pedicle Screw Product Recalled by...
The Issue: The 7mm diameter uniaxial pedicle screws have been color anodized with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemosll ReadiPlasTin (20 ml Size) Recalled by Instrumentation Laboratory Co....
The Issue: Instrumentation Laboratory Co. received customer reports of performance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Saver Elite Processing Kit Recalled by Haemonetics Corporation Due to...
The Issue: Haemonetics has received isolated reports that in some cases the 70ml...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Saver 5/5+ Bowl Set Recalled by Haemonetics Corporation Due to...
The Issue: Haemonetics has received isolated reports that in some cases the 70ml...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JANUS & JANUS G3 Automated Workstation is an automated programmable Recalled...
The Issue: We have become aware through internal testing that JANUS and Janus G3...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The OriGen Reinforced Dual Lumen catheter (RDLC) is a duel Recalled by...
The Issue: Two users have reported to OriGen that a VV28F OriGen Reinforced Dual Lumen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource(R) Kits (custom surgical/procedural kits): The standard and custom...
The Issue: The firm manufactured and distributed Presource(R) kits which contained BD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Segmental System Recalled by Zimmer Biomet, Inc. Due to The products...
The Issue: The products being recalled exceeded the weight previously tested leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versys 6 inch Beaded Full Coat Plus Hip Prosthesis. Labeled Recalled by...
The Issue: The products being recalled exceeded the weight previously tested leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 84" Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical, Inc. Due...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 115" (292 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 185 cm (73") Blood Set w/200 Micron Filter Recalled by ICU Medical, Inc. Due...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 112" (284 cm) 20 Drop Y-Type Blood Set w/200 Micron Filter Recalled by ICU...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 116" (295 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 99" (251 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 162" Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical, Inc. Due...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 168 cm (66") 20 Drop Blood Set w/200 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 100" (254 cm) 20 Drop Y-Type Blood Admin Set w/200 Micron Filter Recalled by...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.