Sandoz recalls 40mg enoxaparin syringes due to temperature issues during shipping that could affect safety. Learn if your product is affected and what to do.
Temperature Abuse; temperature excursion during shipping
Sandoz is recalling enoxaparin sodium injection syringes because they may have been exposed to incorrect temperatures during shipping. This could lead to the medication being unsafe for use.
The syringes may have been exposed to temperatures outside the safe range during shipping. This could cause the medication to become unstable, potentially affecting its safety and effectiveness.
People who have received the recalled syringes for blood thinning treatment. Those with medical conditions requiring regular injections are most at risk.
Check for the product name 'Enoxaparin Sodium Injection, USP, 40 mg/0.4 mL, Single-Dose Syringes with Automatic Safety Device'. Look for the lot number SAB06761A or the expiration date of 04/2023.
Look for the lot number SAB06761A or expiration date 04/2023 on the syringe packaging.
The recall is due to potential temperature issues during shipping, but the product is generally safe if stored properly. Consult your healthcare provider for specific advice.
Check for the lot number SAB06761A or expiration date 04/2023 on the syringe packaging.
The recall does not specify a remedy, so contact your healthcare provider for guidance on next steps.
We’ve drafted a message you can send Sandoz to request your refund or repair — edit it as you like.
Subject: Recall D-0286-2022 — Sandoz Sandoz Hello, I own a Sandoz that is covered by recall D-0286-2022 from Sandoz. 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.
