Abbott Laboratories 22 French Ross Versa-PEG Complete Gastrostomy Kit, an Over-the-Wire PEG Method Featuring Tube Removal without Endoscopy (list # 50520). Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
22 French Ross Versa-PEG Complete Gastrostomy Kit, an Over-the-Wire PEG Method Featuring Tube Removal without Endoscopy (list # 50520).
Brand
Abbott Laboratories
Lot Codes / Batch Numbers
Lots: 01511GZ00, 09769GZ00, 15086GZ00, 19243GZ00, 88824GZ00.
Products Sold
Lots: 01511GZ00, 09769GZ00, 15086GZ00, 19243GZ00, 88824GZ00.
Abbott Laboratories is recalling 22 French Ross Versa-PEG Complete Gastrostomy Kit, an Over-the-Wire PEG Method Featuring Tube Remova due to Gastrostomy and Jejunostomy primary placement kits which may contain components that may not have been adequately sterilized, were distributed.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Gastrostomy and Jejunostomy primary placement kits which may contain components that may not have been adequately sterilized, were distributed.
Recommended Action
Per FDA guidance
The recalling firm notified customers by letter, dated 11/12/04.
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