Cardinal Health Presource Kits: recall status ⚠ Recalls found. Cardinal Health Presource Kits is named in 8 official recalls in our current data:
FDA Class II recall Z-2942-2026 — Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.FDA Class II recall Z-2943-2026 — Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.FDA Class II recall Z-2944-2026 — Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.And 5 more listed below. Source checks: September 7, 2026 at 6:00 AM UTC (oldest successful check).
Sources, dates and coverage limits We collect recent notices on a six-hour schedule using a rolling 90-day source request. Older retained records may also appear. This is a recall index, not a catalogue of all products or a complete recall history.
CPSC: stored recall dates April 30, 2026 to September 3, 2026. NHTSA: stored recall dates April 24, 2026 to September 1, 2026. FDA: stored recall dates April 29, 2026 to August 19, 2026. USDA FSIS is not aggregated here. Check USDA meat, poultry and processed egg notices . EPA and U.S. Coast Guard are not aggregated. Source delays and missing identifiers can prevent a match.
Brand Cardinal Health 200 Recalls naming this model FDA Class II · Medical device · August 19, 2026
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Company / brand: Cardinal Health 200
Affected product: Cardinal Health Presource Kits
Official ID Z-2942-2026 ·
Official record ↗
FDA Class II · Medical device · August 19, 2026
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Company / brand: Cardinal Health 200
Affected product: Cardinal Health Presource Kits
Official ID Z-2943-2026 ·
Official record ↗
FDA Class II · Medical device · August 19, 2026
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Company / brand: Cardinal Health 200
Affected product: Cardinal Health Presource Kits
Official ID Z-2944-2026 ·
Official record ↗
FDA Class II · Medical device · August 19, 2026
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Company / brand: Cardinal Health 200
Affected product: Cardinal Health Presource Kits
Official ID Z-2945-2026 ·
Official record ↗
FDA Class II · Medical device · August 19, 2026
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Company / brand: Cardinal Health 200
Affected product: Cardinal Health Presource Kits
Official ID Z-2946-2026 ·
Official record ↗
FDA Class II · Medical device · August 19, 2026
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Company / brand: Cardinal Health 200
Affected product: Cardinal Health Presource Kits
Official ID Z-2947-2026 ·
Official record ↗
FDA Class II · Medical device · August 19, 2026
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Company / brand: Cardinal Health 200
Affected product: Cardinal Health Presource Kits
Official ID Z-2948-2026 ·
Official record ↗
FDA Class II · Medical device · August 19, 2026
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
Company / brand: Cardinal Health 200
Affected product: Cardinal Health Presource Kits
Official ID Z-2949-2026 ·
Official record ↗
See all Cardinal Health 200 recalls →
Compiled from connected official public-domain government data. Sources last checked September 7, 2026 at 6:00 AM UTC.