Smiths Medical ASD, Inc. A3077-25 SPINAL (SDD) W/DRUGS Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
A3077-25 SPINAL (SDD) W/DRUGS
Brand
Smiths Medical ASD, Inc.
Lot Codes / Batch Numbers
Lot Numbers: K516531, K521703
Products Sold
Lot Numbers: K516531, K521703
Smiths Medical ASD, Inc. is recalling A3077-25 SPINAL (SDD) W/DRUGS due to Trays contain Hospira recalled 2ml drug ampuls of 5% Lidocaine Hydrochloride with 7.5% Dextrose Injection, (NDC 0074-4712-01, lot number 09-568-DK) H. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Trays contain Hospira recalled 2ml drug ampuls of 5% Lidocaine Hydrochloride with 7.5% Dextrose Injection, (NDC 0074-4712-01, lot number 09-568-DK) Hospira, Inc. was recalling the 2ml drug vials of 5% Lidocaine Hydrochloride w/ 7.5% Dextrose lot number 09-568-DK). The drug is being recalled due to reports of particulate in the product.
Recommended Action
Per FDA guidance
Smiths Medical notifed Dealers and direct customers were contacted via letter delivered by Federal Express on July 2, 2004. Customers and dealers are directed to fax back the attached Reply Letter
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026