Hazard
1,010 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 infection risk 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.
Payless Compounders is recalling a compounded semaglutide injectable due to lack of sterility assurance. The recall affects 91 vials distributed in Oregon.
International Medication Systems Ltd. is recalling epinephrine injection due to lack of assurance of sterility. The recall affects 81,520 units of lot EA038A5 distributed nationwide.
Fresenius Kabi USA, LLC is recalling multiple batches of 0.9% sodium chloride intravenous injection due to lack of sterility assurance. No illnesses have been reported, but non-sterile IV solutions pose a risk of serious infection.
Artificial Tears glycerin eye drops made by Preferred Pharmaceuticals are being recalled due to lack of sterility assurance. The 0.5 oz bottles were distributed nationwide.
Fresenius Kabi USA is recalling specific batches of 0.9% sodium chloride injection due to lack of assurance of sterility. The product is distributed nationwide, Alaska, and Puerto Rico.
Fresenius Kabi USA is recalling a batch of 0.9% Sodium Chloride Injection due to lack of assurance of sterility. The product was distributed nationwide, in Alaska, and Puerto Rico.
Medline recalls 9,040 ENFIT G-tube connector kits due to manufacturing defects preventing proper sealing and causing leakage, risking delayed care. Over-tightening to prevent leakage risks infection and additional clinical complications.
Medline is recalling 651,789 ENFIT G-Tube Connectors because they may not form a proper seal with compatible feeding devices, risking leakage that could delay care and cause fluid loss.
Chiesi USA, Inc. is recalling 7,235 vials of CUROSURF (poractant alfa) nationwide due to lack of assurance of sterility. The affected intratracheal injection is used in neonatal care.
Olympus Endoscope Reprocessor OER-Elite is no longer compatible with MAJ-1443 and MAJ-1444 endoscope models. Affected endoscopes may not be properly sterilized when processed in this reprocessor, creating infection risk.
Teva Pharmaceuticals is recalling Octreotide Acetate injectable suspension nationwide due to quality system deficiencies identified at the contract manufacturer that affect assurance of product sterility.
Artelon FLEXBAND TWIST surgical augmentation devices failed bacterial endotoxin testing. The recall affects devices distributed nationwide and internationally; contact your healthcare provider if you received this device.
Medline Industries is recalling surgical drapes that may develop premature fabric delamination during laundering. This could delay patient care or allow surgical site contamination if the affected product is used.
Medline Medcrest surgical gowns may delaminate when laundered, risking surgical barrier failure and infection. The FDA has recalled 104,004 units distributed nationwide and internationally.
Medline is recalling sterile saline wound wash products due to potential failure to meet required sterility assurance levels. The products may not be guaranteed sterile for safe wound care.
Medline has recalled certain Nail Kits because the sterile saline wound wash component may not meet required sterility standards. The affected kits were distributed nationwide and internationally.
Medline is recalling 516 dialysis insertion kits due to silicone seal defects that may block fluid flow or cause therapy delays. Affected units risk allowing biological contamination or air to enter the body.
Medline is recalling 1,640 Nail Kits containing sterile saline wound wash because the manufacturer may not have met minimum sterility assurance levels. The affected kits were distributed nationwide and internationally.
Integra LifeSciences is recalling Medihoney Calcium Alginate wound dressings due to potential packaging failures that could breach the sterile barrier and increase infection risk.
Medline Industries recalled five arthroscopy surgical kit models due to calibration issues with sterilization and packaging equipment that could compromise sterility assurance. The recall affects 175 units distributed nationwide.
Medline is recalling approximately 39,315 surgical device kits due to calibration issues in sterilization equipment that could compromise device sterility. The affected kits are used in cardiac, vascular, and general surgical procedures.
Medline is recalling 779 units of five convenience kit models due to calibration issues in sterilization equipment. These issues may compromise the sterility assurance of affected devices.
Bard is recalling approximately 14,935 central venous catheters (Broviac and Hickman brands) because outer tray damage may compromise the sterile barrier.
Medline Industries, LP is recalling 9,051 surgical device kits due to sterilization equipment calibration issues that could compromise sterility assurance levels. The recalled kits may not be adequately sterile despite undergoing validated sterilization processes.
Medline is recalling 2,740 surgical and biopsy convenience kits due to calibration issues with sterilization equipment that may have compromised product sterility. No injuries have been reported.