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. 2,173 recalls have been distributed to New Jersey in the last 12 months.
Showing 13941–13960 of 29,496 recalls
Recalled Item: BD Vacutainer PST Blood Collection Tubes Recalled by Becton Dickinson &...
The Issue: False elevation of carboxyhemoglobin (COHb) results have been reported when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Lithium HeparinN (LH) 158 USP Units Blood Collection Tubes...
The Issue: False elevation of carboxyhemoglobin (COHb) results have been reported when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PST Gel and Lithium HeparinN (LH) Blood Collection Tubes...
The Issue: False elevation of carboxyhemoglobin (COHb) results have been reported when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PST Gel and Lithium HeparinN (LH) 65 Units Blood Collection...
The Issue: False elevation of carboxyhemoglobin (COHb) results have been reported when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis BA Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A tolerance issue in the power supply of the generator control above a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis dFA Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A tolerance issue in the power supply of the generator control above a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee floor Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A tolerance issue in the power supply of the generator control above a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNCHRON Systems Barbiturates Reagent (BARB 1 X 250) Recalled by Beckman...
The Issue: The firm has identified that cross-reactivity testing may not meet the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Human Assayed Multi-Sera Level 2 Recalled by Randox Laboratories, Limited...
The Issue: The RX Series control target and range value for ALT (Tris buffer without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StemPro¿ MSC SFM CTS" Recalled by Life Technologies Corporation Due to...
The Issue: Component was not tested by the supplier for adventitious agents
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CTSTM Essential 8 Medium Recalled by Life Technologies Corporation Due to...
The Issue: Component was not tested by the supplier for adventitious agents
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView SPECT Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: An issue with the handcontroller may result in either spontaneous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Reverse Shoulder Instrument Case Outer (Outer Case Vault Only)...
The Issue: Lack of an adequate sterilization validation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity ci -series System Control¿Module Recalled by Abbott Gmbh & Co. KG...
The Issue: Abbott has identified an issue with all on market versions (v2.6.0 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Reverse Shoulder Instrument Case Total (Outer Case Vault Only)...
The Issue: Lack of an adequate sterilization validation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X Recalled by Philips Medical Systems (Cleveland) Inc Due to An...
The Issue: An issue with the handcontroller may result in either spontaneous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus WM-NP2 or WM-DP2 Mobile Workstations with Nurse Control Panel Arm...
The Issue: WM-NP/DP2 workstations could become unstable and may fall over if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Recalled by Philips Medical Systems (Cleveland) Inc Due to An...
The Issue: An issue with the handcontroller may result in either spontaneous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luer Lock Set - Catalog # MPC-125 Recalled by Molded Products Inc Due to...
The Issue: Mislabeling - Some unit of sale packages (bags of 100 sets of MPC-125) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thyroid Collar Recalled by Burlington Medical, LLC Due to The protective...
The Issue: The protective material used in the manufacture of the products could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.