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. 2,669 recalls have been distributed to New Jersey in the last 12 months.
Showing 23061–23080 of 29,496 recalls
Recalled Item: HDL-Cholesterol plus gen.3. Recalled by Roche Diagnostics Operations, Inc....
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triglycerides GPO. In vitro test for the quantitative determination of...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cholesterol CHOD-PAP. In vitro diagnostic reagent system intended for use...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LDL-Cholesterol gen.2. The Boehringer Mannheim Direct LDL-Cholesterol test...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cholesterol Gen.2. The cassette COBAS Integra Cholesterol Gen.2 (CHOL2)...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HDL-Cholesterol gen.3. For the quantitative determination of high-density...
The Issue: Possible drug interference when using the Trinder reaction method on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation Due to...
The Issue: Chest drains have a missing o-ring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation Due to...
The Issue: Chest drains have a missing o-ring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rapidlab 1265 system is a blood gas analyzer used Recalled by Siemens...
The Issue: D50 and D51 diagnostic error codes are not functional.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3(TM) 28 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...
The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3(TM) 22 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...
The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3(TM) 22 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...
The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo Workflow SLR Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A potential exists for order transactions from interfaced HIS (Hospital...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3(TM) 22 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...
The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rapidlab 1260 system is a blood gas analyzer used Recalled by Siemens...
The Issue: D50 and D51 Diagnostic error codes are not functional.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Signal Reagent Recalled by ORTHO-CLINICAL...
The Issue: The Immunodiagnostic Products Signal Reagent, Lot 3082 as the reagent packs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen Laboratory Automation System (enGen System) Recalled by Ortho-Clinical...
The Issue: Recapper Caps may fall off of, or be knocked from sample tubes placed in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R3(TM) 28 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...
The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D2-40 (Lymphatic Marker) Recalled by Biocare Medical, LLC Due to Firm...
The Issue: Firm discovered that incorrect Instructions for Use were shipped with one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Astral 100 ( Model No. 27001) & Astral 150 (Model No. 27003) ventilator....
The Issue: The Astral device allows clinicians to disable all alarms including those...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.