State
73,737 recalls have nationwide distribution and so reach New Jersey. 9,780 additional recalls listed New Jersey specifically in their distribution scope.
Of the 9,780 recalls naming New Jersey we have scored against our rubric, 1,246 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,942 (30%) are Severe.
Which agencies issued them
These figures cover only the 9,780 recalls whose distribution notice names New Jersey specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Michigan Herbal Remedies is recalling 486 bottles of Made by Hemp 1000MG Hemp Extract due to elevated levels of undeclared lead.
Michigan Herbal Remedies is recalling A Clean Choice CBD Tincture bottles due to elevated levels of undeclared lead.
Michigan Herbal Remedies is recalling Tasty Drops CBD oil bottles due to elevated levels of undeclared lead.
CareFusion 303, Inc. is recalling Alaris EtCO2 Module Model 8300 units because cleaning agents may damage connectors, potentially interrupting infusion therapy or monitoring.
Active Brands is recalling about 300 Sweet Protection bicycle helmets because they do not meet U.S. safety standards, posing a risk of head injury.
Thule is recalling about 4,000 Sleek strollers because the handlebar can detach, posing an injury hazard to children. No injuries have been reported.
Medline Industries Inc is recalling 1,400 endoscopic cleaning brushes because the brush may detach during use. The recall covers specific models and lots distributed nationwide.
Normand-Info is recalling Remisol Advance software version 1.12 because it deletes specific white blood cell and platelet results, potentially leading to erroneous data.
Winnebago is recalling certain 2021 Revel motorhomes. The auxiliary alternator belt may wear and detach, which could cause loss of power steering control and increase the risk of crashes.
Siemens is recalling 49 Luminos dRF Max units due to software defects that may cause system collisions or incorrect diagnostic images.
Boss Instruments is recalling 96 DeBakey needle holders because the tungsten carbide plate can break under pressure, posing a risk to patients and medical staff.
Teleflex Medical Inc. is recalling Pleur-Evac chest drainage devices because sterile packaging may be compromised, potentially affecting sterility.
CPSC warns consumers to stop using and dispose of Crown Darts UK lawn dart sets because they are banned in the U.S. due to serious injury risks.
Becton Dickinson is recalling BD MAX SARS-CoV-2 Reagents due to elevated rates of potential false positive results, which could delay diagnosis and increase exposure risk.
Siemens Medical Solutions is recalling 477 Luminos Agile Max units due to software defects that may cause system collisions or incorrect diagnostic images.
Siemens is recalling 194 Uroskop Omnia Max units due to software issues that may cause system collisions or incorrect diagnostic images.
Intertex is recalling approximately 189,000 B-Air, BlueDri, BlueDri Pro, and Soleaire blowers because unprotected side outlets pose a fire hazard.
Randox Laboratories is recalling specific batches of Lipase R2 Substrate due to confirmed imprecision in quality control and patient samples.
Teleflex Medical Inc. is recalling Pleur-Evac chest drainage devices because sterile packaging may be compromised, potentially affecting sterility.
Siemens Healthcare is recalling 1,800 DCA Vantage Handheld Barcode Scanners because they may fail to verify check digits or incorrectly process barcodes, potentially leading to data errors.
Randox Laboratories is recalling specific batches of Lipase Colorimetric R1 Buffer due to confirmed imprecision in quality control and patient samples.
Vilvet Pharmaceuticals is recalling 11,640 bottles of VILAMIT MB capsules due to current Good Manufacturing Practice (cGMP) deviations. The recall is voluntary and nationwide.
Randox Laboratories is recalling specific batches of Lipase Colorimetric Reagent due to confirmed imprecision in quality control and patient samples.
Smith & Nephew is recalling 868 units of SUTUREFIX ULTRA Suture because a packaging error caused an XL drill to be included instead of the correct S drill.
Sutter Medizintechnik GmbH is recalling 1,337 units of Sutter Swyng non-stick bipolar forceps because the package insert incorrectly displays the Ethylene Oxide sterilization symbol instead of the irradiation symbol.