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Punjab Halts Eight IV Fluid and Injection Batches After Adverse Reaction Reports

Officials described a precautionary step following suspected adverse reactions, with laboratory testing plus a PHSC review underway.

Overview

  • The health department ordered government hospitals to stop use, distribution and procurement of the named batches immediately and to isolate any existing stock.
  • The directive lists specific products and batches, including Normal Saline, Dextrose 5%, Ciprofloxacin 200 mg, DNS 0.9%, N/2 + Dextrose 5%, and Bupivacaine HCL with Dextrose, with expiries running through 2026–2028.
  • The suspended batches were manufactured by Swaroop Pharmaceuticals, Otsuka Pharmaceutical India and Health Biotech, according to the official memo.
  • A committee under the Punjab Health Systems Corporation was tasked to evaluate the suspected adverse drug reactions, while samples from the flagged batches were dispatched for lab analysis.
  • Hospitals were warned of departmental action for non‑compliance, as the suspension follows a recent Coldrif syrup ban and earlier IV‑fluid recalls that have sharpened scrutiny of procurement and quality controls.