Hazard
41 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 41 sterility documentation recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.
Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all sterility documentation 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.
Wright Medical Technology is recalling 77 units of Dart Fire Headed Screws because the firm discovered a lack of adequate documentation confirming sterility.
Wright Medical Technology is recalling 19 units of PRO-STIM 10cc Injectable because adequate documentation confirming sterility was missing.
Wright Medical Technology is recalling 40 units of Ortholoc 3DI locking screws because documentation confirming sterility was inadequate.
Wright Medical Technology is recalling 20 Swanson Trapezium Implants because the firm discovered a lack of adequate documentation confirming sterility.
Wright Medical Technology is recalling 30 units of Evans Opening Wedge Plates because documentation confirming sterility was inadequate.
Wright Medical Technology is recalling 65 units of INBONE STEM, TIBIAL, TOP components because adequate documentation confirming sterility was not found.
Wright Medical Technology is recalling 54 units of Valor Screws because adequate documentation confirming sterility was missing.
Wright Medical Technology is recalling 66 units of sterile headed drill bits because documentation confirming sterility was inadequate.
Wright Medical Technology is recalling 20 units of Swanson Finger Joint #1 implants because documentation confirming sterility was inadequate.
Wright Medical Technology is recalling 42 units of CPS Calcaneal Plates because the firm discovered a lack of adequate documentation confirming sterility.
Wright Medical Technology is recalling 18 units of Swanson Finger Joint #2 implants because documentation confirming sterility was inadequate.
International Medsurg Connection, Inc. is recalling 54,204,100 units of piston syringes and hypodermic needles because of insufficient documentation to support sterility claims.
International Medsurg Connection, Inc. is recalling hypodermic needles because the company lacks sufficient documentation to support the products' sterility claims.
International Medsurg Connection is recalling hypodermic needles because the company lacks documentation to support the products' sterility claims.
International Medsurg Connection, Inc. is recalling 54,204,100 units of piston syringes and hypodermic needles because documentation supporting sterility claims is insufficient.
International Medsurg Connection is recalling 54,204,100 hypodermic needles because the company lacks sufficient documentation to support the product's sterility claims.
International Medsurg Connection, Inc. is recalling 60 CC Syringe Bulbs because the company lacks sufficient documentation to support the product's sterility claims.
International Medsurg Connection, Inc. is recalling 54,204,100 units of piston syringes and hypodermic needles because the company lacks sufficient documentation to support the products' sterility claims.
International Medsurg Connection, Inc. is recalling hypodermic needles because the company lacks sufficient documentation to support the products' sterility claims.
International Medsurg Connection, Inc. is recalling 54,204,100 piston syringes and hypodermic needles nationwide because of insufficient documentation to support product sterility claims.
International Medsurg Connection, Inc. is recalling 54,204,100 piston syringes and hypodermic needles because the company lacks sufficient documentation to support product sterility claims.
International Medsurg Connection, Inc. is recalling 54,204,100 piston syringes because the company lacks sufficient documentation to support product sterility claims.
International Medsurg Connection, Inc. is recalling 54,204,100 hypodermic needles because the company lacks sufficient documentation to support the products' sterility claims.
International Medsurg Connection, Inc. is recalling 54,204,100 piston syringes because the company lacks sufficient documentation to support the product's sterility claims.
International Medsurg Connection, Inc. is recalling 16-gauge hypodermic needles because the company lacks sufficient documentation to support the product's sterility claims.