Hazard
37 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.
Of the 37 incompatibility recalls we have scored against our rubric, 2 (5%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2 (5%) are Severe.
Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all incompatibility 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.
FDA recalls 133,930 pairs of Kendall defibrillation electrodes because they are not compatible with specific Philips AED models.
FDA recalls 31,590 pairs of Kendall defibrillation electrodes because they are not compatible with Philips FR3 or FRx AEDs.
Covidien is recalling Philips HEARTSTART Multifunction Electrode Pads because they are not compatible with Philips FR3 or FRx AEDs.
Coviden LLC is recalling 9,850 pairs of Medi-Trace Cadence defibrillation electrodes because they are not compatible with Philips FR3 or FRx AEDs.
The FDA is recalling 330 pairs of MediChoice Multifunction Electrodes because they are not compatible with certain Philips AED models.
Stryker is recalling 41 sterile neuro drill accessories due to missing or partial notches that may affect compatibility with Elite attachments.
SpineFrontier, Inc. is recalling 23 Arena-L 35x26 Trial Heads because they may not be compatible with the trial handles.
SpineFrontier, Inc. is recalling 23 Arena-L trial heads because they may not be compatible with the trial handles.
SpineFrontier, Inc. is recalling 23 Arena-L Trial Handles and Heads because the components may not be compatible. The devices were distributed only to the U.S. Department of Veterans Affairs.
AdvanDx is recalling Gram-Negative QuickFISH BC kits because they are incompatible with certain fluorescence microscope light sources.
Aesculap, Inc. is recalling 24 Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7, because they were not compatible.
ConMed is recalling WANG Transbronchial Aspiration Needles because they may not fit through a 2.0 mm bronchoscope, causing minor inconvenience.