Synthetopes recalls Pentreotide (10 uGm) due to lack of processing controls. All lots within expiry are affected. Consumers should contact the manufacturer for details.
Lack of Processing Controls.
Synthet:opes is recalling Pentreotide (10 uGm) because of processing control issues. This could affect product safety, though the exact risk isn't specified in the recall.
The recall states there's a lack of processing controls, which could lead to unsafe product conditions. However, the specific hazard mechanism isn't detailed in the notice.
People who have the Pentreotide (10 uGm) product from Synthetopes Inc are affected. The recall applies to all lots within expiry.
Check for Pentreotide (10 uGm) from Synthetopes Inc. All lots within expiry are included in this recall.
Reach out to Synthetopes Inc for specific instructions on handling the recalled product.
The recall states there's a lack of processing controls, but doesn't specify if the product is safe to use.
Look for Pentreotide (10 uGm) from Synthetopes Inc. All lots within expiry are affected.
Contact Synthetopes Inc for specific instructions on handling the recalled product.
We’ve drafted a message you can send Synthetopes to request your refund or repair — edit it as you like.
Subject: Recall D-1399-2019 — Synthetopes Synthetopes Hello, I own a Synthetopes that is covered by recall D-1399-2019 from Synthetopes. 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.
