3M Ioban 2 Antimicrobial Incise Drapes, Model 6648EZ Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
3M Ioban 2 Antimicrobial Incise Drapes, Model 6648EZ
Lot Codes / Batch Numbers
3M Ioban 2 Antimicrobial Incise Drapes, Model 6648EZ, which were contained in Cardinal Health Custom Procedure Packs sterilized between December 20, 2002 and February 28, 2003, were recalled.
Products Sold
3M Ioban 2 Antimicrobial Incise Drapes, Model 6648EZ, which were contained in Cardinal Health Custom Procedure Packs sterilized between December 20, 2002 and February 28, 2003, were recalled.
A medical device manufacturer is recalling 3M Ioban 2 Antimicrobial Incise Drapes, Model 6648EZ due to The product did not meet its specifications for iodine content, and had the possibility of causing moderate short-term skin irritation if used.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The product did not meet its specifications for iodine content, and had the possibility of causing moderate short-term skin irritation if used.
Recommended Action
Per FDA guidance
3M sent Cardinal Health a letter dated April 7, 2003 to provide to their customers. The letter instructed the customers to remove Ioban 2 drapes contained in Cardinal Health packs and use a separately supplied equivalent drape.
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