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 28441–28460 of 29,496 recalls
Recalled Item: Multipolar¿ Bipolar Cup Liner 22 mm LD. Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Inc. is initiating a removal of the Multipolar¿ Bipolar Cup Liner 22...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Brilliance CT Big Bore is a whole-body Computed Tomography Recalled by...
The Issue: Philips Healthcare received a complaint stating the system opens e-stop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREMIER(R) Anterior Cervical Plate System SCREW BLOCK Recalled by Medtronic...
The Issue: Lines on the screw gauge may not placed on the caddy properly which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATLANTIS(R) Anterior Cervical Plate System VARIABLE ANGLE SCREW MODULE...
The Issue: Lines on the screw gauge may not placed on the caddy properly which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATLANTIS(R) Anterior Cervical Plate System FIXED ANGLE SCREW MODULE Recalled...
The Issue: Lines on the screw gauge may not placed on the caddy properly which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guardian II Hemostasis Valve Recalled by Vascular Solutions, Inc. Due to...
The Issue: Vascular Solutions, Inc., became aware of a potential problem involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq Two Channel Infuser Recalled by Hospira Inc. Due to The Symbiq pump...
The Issue: The Symbiq pump touchscreen may not respond to user selection, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Automatic Cutting Needles Recalled by Remington Medical Inc. Due to...
The Issue: Sterility of the product may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq One Channel Infuser Recalled by Hospira Inc. Due to The Symbiq pump...
The Issue: The Symbiq pump touchscreen may not respond to user selection, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Brilliance CT 16 System Product Usage: The Brilliance 16 Recalled by...
The Issue: Philips was notified that the system logout in software version 2.3.6 is now...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sekisui Spectrolyse PAI-1 Recalled by Sekisui Diagnostics Llc Due to...
The Issue: SPECTROLYSE PAI-1 activity assay producing lower than expected absorbance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREVI Isola System Recalled by Biomerieux Inc Due to The instrument may not...
The Issue: The instrument may not dispense the specimen onto the pre-poured media...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TORQ Sternal Closure Device. The common name is TWISTER Recalled by Kardium...
The Issue: The TORQ Sternal Closure Device, Lot 062711, is being recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spine Frontier Inspan compressors Part Number: 11-60004. Inspan compressors...
The Issue: Inspan Compressors may break at weld causing a loss of compression
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empty Evacuated Container 250 mL and 1000 mL. Empty Evacuated Recalled by...
The Issue: Embedded iron oxide glass defect which may have the potential to break off...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy II Constrained Liner The Trilogy Longevity Constrained Liner serves...
The Issue: Trilogy Longevity Constrained Liner devices were packaged in incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MX 16-slice CT Scanner System Recalled by Philips Medical Systems...
The Issue: On August 24, 2012 the firm recalled the MX 16-slice after discovering that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The brand name is MRidium Series 1000 MR Infusion Sets Recalled by Iradimed...
The Issue: Iradimed Corporation is recalling MRidium Series 1000 MR Infusion Sets, Type...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optilock 2.7 mm Screw Inserter. 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: Universal Flex2 Breathing Circuit Class I 510(k) Exempt An anesthesia...
The Issue: King Systems received a customer complaint indicating that the customer had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.