State
73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
CSM Bakery Products is recalling 35 lb. pails of Vanilla Xtra Smooth Buttercreme Frosting because pieces of plastic polymer were introduced into the sugar system.
Nobel Biocare is recalling 233 units of Abutment Screw Retrieval Instruments because a packaging defect may compromise sterility during shelf life.
Smith & Nephew is recalling TwinFix Ti 2.8 mm HS Suture Anchors because a protective tube failure may have breached the sterile barrier.
Siemens Medical Solutions is recalling 96 ARTIS Pheno-Interventional Fluoroscopic X-Ray Systems because safety brakes may block the robotic stand, preventing intended movements.
Nobel Biocare is recalling specific tapered dental drills because a packaging defect may compromise their sterility during shelf life.
CSM Bakery Products is recalling frozen chocolate chip cookie dough because pieces of plastic polymer were introduced into the sugar system.
American Health Packaging is recalling Desmopressin Acetate Tablets because product bottles may be missing desiccant.
The FDA is recalling specific lots of Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that could compromise the sterility barrier.
Nobel Biocare is recalling 260 units of tapered dental drills because a packaging sealing issue may compromise sterility during shelf life.
The FDA is recalling specific lots of Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that could impact the humidity or sterility barrier.
Nobel Biocare is recalling 87 units of Implant Retrieval Kits because a packaging sealing issue may compromise the sterility of the devices during their shelf-life.
Ormco/Sybronendo is recalling SnapLink brackets because the lower buccal tube slide doors may not stay closed, potentially causing tooth rotation and treatment delays.
Abbott Point Of Care Inc. is recalling i-STAT CG4+ cartridges because they are not FDA cleared and lack CLIA waived status.
Covidien LLC is recalling Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that may impact the humidity or sterility barrier.
American Health Packaging is recalling Desmopressin Acetate Tablets because the product bottles may be missing desiccant.
Abbott Point Of Care Inc. is recalling i-STAT CHEM8+ cartridges because they are not FDA cleared and do not have CLIA waived status.
Suja Life LLC is recalling 7,660 bottles of Organic Berry Zest Fruit + Veggie Smoothie due to an unapproved herbicide found in raw flax material.
Suja Life LLC is recalling 8,798 bottles of Organic Tropical Dragon Fruit + Veggie Smoothie due to an unapproved herbicide in raw flax material.
Arrow International Inc. is recalling 1,320 units of the Arrow Epidural Catheterization Kit because the product lidstock contains the incorrect expiration date.
Arrow International Inc. is recalling 1,360 units of the Arrow Epidural Catheterization Kit CK-02220 because the product lidstock contains the incorrect expiration date.
Nobel Biocare is recalling 2,470 implant retrieval instruments because a packaging defect may compromise sterility. The devices are distributed worldwide.
Nobel Biocare is recalling 8 Dense Bone Drills because a packaging defect may compromise sterility during shelf life.
Nobel Biocare is recalling 59 dental drills because a packaging defect may compromise sterility. The devices are distributed worldwide.
Arrow International Inc is recalling 2,126 units of STIM and INSL CPNB Tuohy needles because the product lidstock contains the incorrect expiration date.
Siemens Healthcare Diagnostics is recalling Atellica CH High Sensitivity C-Reactive Protein Calibrators for in vitro diagnostic use.