Class II · Moderate risk Ongoing
Baclofen Tablets USP
Reason Presence of Foreign Tablets/Capsules
All baclofen Products
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of Processing Controls
What was recalled
All baclofen Products, Rx Only, Compounded by RELIABLE DRUG/RELIABLE COMPOUNDING PHARMACY, 801 Irving St., SAN FRANCISCO, CA 94122.
- Recalling firm
- Reliable Rexall-A Compounding Pharmacy
- Origin
- CA, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-1134-2016
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Baclofen recalls
See all
Class I · High risk Terminated
Sufentanil-Bupivacaine-Baclofen Pf 25mcg-12.5mg-750mcg/Ml…
Reason Non-Sterility
Class I · High risk Terminated
HYDROMORPHONE HCL-BUPIVACAINE HCL-BACLOFEN PF INJECTABLE 21 mL…
Reason Non-Sterility
Class I · High risk Terminated
Fentanyl-Bupivacaine Hcl-Baclofen Pf Injectable 575mcg-18mg-6000mcg/Ml
Reason Non-Sterility
Class I · High risk Terminated
Bupivacaine Hcl-Baclofen Pf Injectable 40mg-4000mcg/Ml
Reason Non-Sterility
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