Hazard
28 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 28 structural integrity recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 9 (32%) are Severe.
Which agencies issued them
Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all structural integrity recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.
A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.
International Motors is recalling 2025-2027 IC Bus CECB transit buses because driver's window and door joints may lack sufficient epoxy, failing federal safety standards.
Bolts and plastic parts of cable hose carriers on Philips Azurion X-ray systems may loosen or break during monitor movement or rotation, potentially causing the cable hose to become unsecured.
Forest River Bus is recalling 2026 Collins school buses because body panel adhesive may be applied incorrectly, causing panels to separate and reducing structural integrity.
Forest River Bus is recalling 2026 Collins Bus transit buses because body panel adhesive may be applied incorrectly, causing panels to separate and reducing structural integrity.
North American Rescue is recalling 552 Junctional Emergency Treatment Tools over a potential manufacturing defect that may compromise structural integrity and performance during use.
About 1,160 sling carriers sold on Walmart.com through Joybuy Marketplace Express are recalled due to violations of federal safety standards. The carriers pose suffocation and fall hazards to infants because they lack required structural integrity, occupant retention, and proper restraint systems.
Zimmer, Inc. is recalling certain G7 Acetabular System acetabular shells (52 MM and 60 MM) because the outer sterile package has corner walls thinner than specification, which could crack during transit and potentially lead to surgical complications or infection.
Cardinal Health is recalling approximately 29.8 million lab coats and isolation gowns due to potential manufacturing defects such as rips, holes, and foreign material.
TriMed Inc. is recalling 583 Olecranon Hook Plates because angled holes may have been modified from specifications without full qualification.
TriMed Inc. is recalling 5 Dorsal Wrist Hook Plates due to unqualified design modifications that may compromise structural integrity.
Biomet 3i is recalling 6 units of Certain Bellatek Titanium Abutments because a manufacturing defect causes the screw head to seat too deep without a positive stop.
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a manufacturing rework process caused set screws and sleeves to shift, potentially preventing proper assembly.
Zimmer Biomet is recalling 638 Affixus Hip Fracture Nails because a set screw and sleeve assembly may not be in the correct location, potentially preventing proper product assembly.
C2 Therapeutics is recalling 755 C2 CryoBalloon Controller Caps because they may crack when tightened, potentially compromising the device's integrity.
Ford is recalling 2016 Focus and C-Max vehicles because improperly welded floor pan joints may reduce structural integrity, increasing injury risk in a crash.
Smith & Nephew is recalling 5,806 Tandem hip shell units manufactured with out-of-specification retainer grooves. The recall covers distribution in the US and 23 other countries.
Prevost is recalling 2015-2016 X3-45 buses because cracks in sliding passenger seats may compromise structural integrity, increasing injury risk in crashes.
Microport Orthopedics is recalling 17 units of the Evolution Tibial Base knee prosthesis component due to a casting tool issue causing varying retaining wall thickness and keel offset.
GE Healthcare is recalling 13 Revolution CT scanners to perform a required torque check on three bolted joints. No injuries or illnesses have been reported.
Smith & Nephew is recalling 24 units of the Legion COCR Constrained Femoral Component because the stem taper is undersized and the gauge point is not deep enough.
Goya Pink Beans are being recalled due to a possible can seam defect that may compromise product integrity.
Tradewind Foods is recalling Goya Black Beans due to a possible can seam defect that may compromise product integrity.
Nissan is recalling 2014 Leaf vehicles because missing welds on the front structural member may reduce crash protection. Owners should contact a dealer for a free inspection and repair.
Carestream Health is recalling Kodak 2200 Intraoral X-Ray Systems because the device arms may break early. This affects 347 units distributed in the US and Canada.
Cordis Corporation is recalling 250 units of FLEXSTENT stent systems because holes or tears can form in the protective pouches.