Hazard
1,428 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all class ii 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.
J. Higgs Potato Chip Mix, 18 one-ounce singles per bag, is being recalled because of undeclared milk. 2,275 bags are affected.
Orange Cream Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.
Levothyroxine Sodium Tablets, USP 50 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 54,227 bottles affected.
Levothyroxine Sodium Tablets, USP 175 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 2,344 bottles affected.
Rich Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.
Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with Powder Fresh Scent is being recalled because of CGMP deviations. 21,265 cases are affected.
NeuroSync EYE-SYNC systems containing Pico Neo 2 headsets are being recalled because eye syncing issues render the device inoperable and it cannot be repaired. 27 units are affected.
Beauty & Skincare Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant/Deodorant Spring Fresh is being recalled because of CGMP deviations. 22,482 cases are affected.
Medtronic SmartLink software on the CareLink SmartSync Device Manager is being updated because the system could display an erroneous electrical reset message on interrogation when no reset had occurred. 5,418 units affected.
KWIK-STIK and LYFO DISK quality control kits for culture media are being recalled because affected products contain Staphylococcus epidermidis instead of the expected Brevundimonas diminuta. 21 units affected.
Medtronic SmartLink Software on the SmartSync Patient Connector is being updated because the system could display an erroneous electrical reset message on interrogation when no reset had occurred. 3,909 units affected.
Two bags of compounded Peripheral Parenteral Nutrition are being recalled because a daily cleaning step in the ISO-5 compounding area was not sufficiently documented.
Lisdexamfetamine Dimesylate Capsules 60 mg are being recalled because an out of specification result was observed in dissolution testing at the nine month long term stability station. 5,448 bottles affected.
Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant/Deodorant is being recalled because of CGMP deviations. 23,467 cases are affected.
Wegmans brand Chocolate Chip Mini Muffins are being recalled because the product may contain foreign objects of metal origin. 8,508 units are affected.
Crown Point Shelled Edamame in 22 lb cases is being recalled because the label declares shelled edamame but does not specify or declare soy. 1,046 cases are affected.
VersaCross Access Solution kits are being recalled because of a potential hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. 14,724 units affected.
Wegmans brand Blueberry Mini Muffins family pack is being recalled because the product may contain foreign objects of metal origin. 8,508 units are affected.
C Sweet Ghouribeh with Pistachios is being recalled because soy is undeclared and the contains statement, though present, does not list pistachios. 30 units are affected.
C Sweet Sweet Kaak is being recalled because of undeclared wheat. 20 units are affected, distributed in Michigan.
Torflex Transseptal Guiding Sheath Kits are being recalled because of a potential hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. 14,724 units affected.
Duloxetine Delayed-Release Capsules 40 mg are being recalled because N-nitroso-duloxetine was present above the FDA recommended interim limit. 12,242 bottles are affected.
C Sweet Ghouribeh Rolls with date, sesame and pistachios are being recalled because wheat, soy and sesame are undeclared. 30 units are affected.
Alcon Constellation Vision System Vitrectomy Procedure Paks are being recalled because some units within specific lots may have been damaged during manufacture in the lidding area. 198,205 units affected.
Alcon Custom Paks, customer-designed sterile surgical kits, are being recalled because some units within specific lots may have been damaged during manufacture in the lidding area. 15,557 kits affected.