Medline spinal anesthesia and nerve block kits recalled for bupivacaine quality and efficacy concerns
Medline spinal anesthesia kits recalled for quality issues
Medline distributed multiple spinal anesthesia and nerve block procedure kits containing Bupivacaine Hydrochloride in Dextrose Injection made by Huons Co. The anesthetic was recalled due to quality concerns, including problems with microbiology testing data and reports that the medication may not work as expected.
- If your facility received any Medline spinal procedure kits (SKU DYNJRA or PAIN/SAMPA series), check the lot numbers against the FDA notice
- Do not use affected kits for patient procedures
- Contact Medline at the phone number on your product documentation or the FDA for instructions on returning or disposing of recalled kits
- Consult your anesthesiologist or pharmacist if you have questions about alternative products
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2232-2026Also reported as
- FDA-Device2026-06-03Medline nerve block kits recalled for bupivacaine quality and efficacy concerns
- FDA-Device2026-06-03Medline spinal block trays recalled for bupivacaine quality and efficacy concerns
- FDA-Device2026-06-03Medline anesthesia and spinal anesthesia trays recalled for bupivacaine quality issues
- FDA-Device2026-06-03Medline spinal anesthesia kits recalled for bupivacaine quality and efficacy concerns
- FDA-Device2026-06-03Medline spinal anesthesia trays recalled for bupivacaine quality and efficacy concerns
- FDA-Device2026-06-03Medline spinal block kits recalled for quality and microbiology testing integrity issues
More Medline Industries, LP recalls
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