Aspiro Pharma Limited recalls Ketorolac injection vials with glass particles that could cause serious injury if injected. Affected lots manufactured between 2022-2026. Contact for return instructions.
Presence of Particulate Matter: Particulate matter identified as glass
Aspiro Pharma Limited is recalling Ketorolac injection vials that contain glass particles. Using these vials could cause serious injury if the medication is injected. This recall affects specific production lots with expiration dates through 2026.
Glass particles in the injection vials could cause serious injury when injected into the body. This risk occurs because the particles may enter the bloodstream during administration, potentially causing tissue damage or other complications.
Prescription patients using Ketorolac injections for pain management. Healthcare providers who have the recalled vials are most at risk.
Check the vial label for lot numbers: AS1240347A (exp 09/2026), AS1240144A (exp 05/2026), AS1240145A/AS1240146A (exp 06/2026), or AS1250295A (exp 05/2027). The product is a 2 mL single-dose vial for intramuscular use only.
Immediately discard the vial if it contains glass particles, as injection could cause serious injury.
The recall is due to glass particles found in the injection vials that could cause serious injury if injected.
Affected lot numbers include AS1240347A (exp 09/2026), AS1240144A (exp 05/2026), AS1240145A/AS1240146A (exp 06/2026), and AS1250295A (exp 05/2027).
Check the vial label for the specific lot numbers listed above. The product is a 2 mL single-dose vial for intramuscular use only.
We’ve drafted a message you can send Aspiro Pharma Limited to request your refund or repair — edit it as you like.
Subject: Recall D-0036-2026 — Aspiro Pharma Limited Aspiro Pharma Limited Hello, I own a Aspiro Pharma Limited that is covered by recall D-0036-2026 from Aspiro Pharma Limited. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
