PEMRYDI RTU (pemetrexed injection): recall status ⚠ Recalls found. PEMRYDI RTU (pemetrexed injection) is named in 2 official recalls in our current data:
FDA Class II recall D-0764-2026 — Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vialsFDA Class II recall D-0765-2026 — Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials Source checks: October 22, 2026 at 12:00 PM 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 October 22, 2026. NHTSA: stored recall dates April 24, 2026 to October 19, 2026. FDA: stored recall dates April 29, 2026 to October 14, 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 Shilpa Medicare Also listed as PEMRYDI RTU(pemetrexed injection) Recalls naming this model FDA Class II · Drug · August 26, 2026
Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials
Company / brand: Shilpa Medicare recalls
Affected product: PEMRYDI RTU (pemetrexed injection) recall status
Official ID D-0764-2026 ·
Official record ↗
FDA Class II · Drug · August 26, 2026
Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials
Company / brand: Shilpa Medicare recalls
Affected product: PEMRYDI RTU(pemetrexed injection) recall status
Official ID D-0765-2026 ·
Official record ↗
See all Shilpa Medicare recalls →
Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 12:00 PM UTC.