Isomeric Pharmacy Solution, LLC recalls Betamethasone Acetate / Betamethasone Sodium Phosphate Injectable Suspension, 7 mg/ mL,10 mL Multi-Dose vial for
Lack of processing controls: Isomeric Pharmacy Solution, LLC is recalling Betamethasone Acetate / Betamethasone Sodium Phosphate 7 mg/mL INJ SUSP because of the potential of drug clumps in the vial of the sterile drug product and larger particle sizes.
Recall notice
Lack of processing controls: Isomeric Pharmacy Solution, LLC is recalling Betamethasone Acetate / Betamethasone Sodium Phosphate 7 mg/mL INJ SUSP because of the potential of drug clumps in the vial of the sterile drug product and larger particle sizes.
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Source Page by GovInfoNow · govinfonow.com/recall/42506-isomeric-pharmacy-solution-llc-recalls-betamethasone-acetate-betamethasone-sodium-phosphate · Recall date August 1, 2016 · FDA enforcement record: FDA #D-1454-2016
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“Isomeric Pharmacy Solution, LLC recalls Betamethasone Acetate / Betamethasone Sodium Phosphate Injectable Suspension, 7 mg/ mL,10 mL Multi-Dose vial for.” GovInfoNow, recall dated August 1, 2016. https://govinfonow.com/recall/42506-isomeric-pharmacy-solution-llc-recalls-betamethasone-acetate-betamethasone-sodium-phosphate. Based on FDA recall #D-1454-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1454-2016%22&limit=1).
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We’ve drafted a message you can send Isomeric Pharmacy Solution, LLC to request your refund or repair — edit it as you like.
Subject: Recall D-1454-2016 — Isomeric Pharmacy Solution, LLC Isomeric Pharmacy Solution, LLC recalls Betamethasone Acetate / Bet Hello, I own a Isomeric Pharmacy Solution, LLC recalls Betamethasone Acetate / Betamethasone Sodium Phosphate Injectable Suspension, 7 mg/ mL,10 mL Multi-Dose vial for that is covered by recall D-1454-2016 from Isomeric Pharmacy Solution, LLC. 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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Where this comes from
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.
- Official source: FDA Recall #D-1454-2016 (August 1, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1454-2016 to see it in context.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.