IV Flush LLC Sodium Chloride Injection USP, manufactured by IV Flush LLC Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Sodium Chloride Injection USP, manufactured by IV Flush LLC
Brand
IV Flush LLC
Lot Codes / Batch Numbers
All lots remaining on the market.
Products Sold
All lots remaining on the market.
IV Flush LLC is recalling Sodium Chloride Injection USP, manufactured by IV Flush LLC due to Device marketed without 510(k) clearance and is suspected to be contaminated with P. Flourescens.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Device marketed without 510(k) clearance and is suspected to be contaminated with P. Flourescens.
Recommended Action
Per FDA guidance
The firm initiated the recall by fax to distributors on 01/26/2005. On 2/16/2005 the firm faxed a second recall letter with return reciept response card to all consignees.
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