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. 2,642 recalls have been distributed to New Jersey in the last 12 months.
Showing 28461–28480 of 29,496 recalls
Recalled Item: Optilock T15 AO Driver (3.5mm). Intended Use: The OptiLock Upper Recalled by...
The Issue: Field complaints indicate that recent shipments of the 14-400795 and 36505...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-Rom¿ Total Hip System Poly Liner Packaging: The insert is Recalled by...
The Issue: Orthopaedics, Inc. (DePuy) is issuing a voluntary recall of four lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12/14 TAPER HIGH OFFSET NECK USE WITH SMITH & NEPHEW Recalled by Smith &...
The Issue: Modular necks were manufactured out of specification by a vendor; the taper...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-Lift Implant Guides (also known as S-LIF) Compressor Part Number: Recalled...
The Issue: When using the optional S-LIFT (also known as S-LIF) Implant Guides without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Tip Marker Recalled by Viscot Medical LLC Due to Dual Tip Marker has...
The Issue: Dual Tip Marker has inconsistent ink flow on the black permanent ink side.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHICON SURGIFLO HEMOSTATIC MATRIX KIT Plus FlexTip with Thrombin...
The Issue: SURGIFLO Hemostatic Matrix Kit & SURGIFLO Hemostatic Matrix Kit with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETHICON SURGIFLO HEMOSTATIC MATRIX Distributed by ETHICON ETHICON Recalled...
The Issue: SURGIFLO Hemostatic Matrix Kit & SURGIFLO Hemostatic Matrix Kit with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Mobilett Mira. Mobile X-Ray System. Recalled by Siemens Medical...
The Issue: During regular product monitoring, Siemens has become aware of a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oncentra External Beam 4.1. Radiation treatment planning software designed...
The Issue: During the planning process the beam weights can be changed by the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Test Discs Recalled by Remel Inc Due to...
The Issue: The firm is recalling the product due to some cartridges may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vycor Medical ViewSite Brain Access System 17mm/ 11mm / 5cm Recalled by...
The Issue: Vycor Medical recalled their VBAS (Vycor Viewsite Brain Access System)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-Ray Systems Recalled by Philips Medical Systems...
The Issue: A bolt which attaches the oil accumulator within the gantry may fail,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Antimicrobial Susceptibility Discs Recalled by Remel Inc Due to The...
The Issue: The firm is recalling the product because the cartridges may contain discs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermo Scientific MAS Omni IMMUNE and Omni IMMUNE PRO Recalled by...
The Issue: In house testing confirmed that CK-MS and Insulin claimed in both Omni...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Xpect Clostridium difficile Toxin A/B Recalled by Remel Inc Due to The...
The Issue: The firm is recalling the products due to a potential for false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Armada 35/ Armada 35 LL PTA Catheters. The device is Recalled by Abbott...
The Issue: Abbott Vascular is recalling the Armada 35 and Armada 35 LL PTA Catheters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Xpect Clostridium difficile Toxin A/B Recalled by Remel Inc Due to The...
The Issue: The firm is recalling the products due to a potential for false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian brand Eclipse Treatment Planning System Recalled by Varian Medical...
The Issue: Varian has identified an anomaly with the Eclipse Treatment Planning where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Octopus 101 Perimeter Recalled by Haag-Streit USA Inc Due to The firm...
The Issue: The firm recalled the device after learning of a possible deviation in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Torx 6.5mm Cancellous Bone Screw The Recalled by...
The Issue: Stryker has received reports from the field indicating that certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.