Boehringer Laboratories Inc Autovac TL. Autotransfusion System for Orthopedic Wound Drainage. The product is shipped in cartons containing 6 units Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Autovac TL. Autotransfusion System for Orthopedic Wound Drainage. The product is shipped in cartons containing 6 units
Brand
Boehringer Laboratories Inc
Lot Codes / Batch Numbers
Model 7924. Lot number 200309 exp. 9/2005
Products Sold
Model 7924. Lot number 200309 exp. 9/2005
Boehringer Laboratories Inc is recalling Autovac TL. Autotransfusion System for Orthopedic Wound Drainage. The product is shipped in cartons due to Inadequate bond where the tube attaches to the inlet of the bulb.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Inadequate bond where the tube attaches to the inlet of the bulb.
Recommended Action
Per FDA guidance
On 11/7/03, the recalling firm contact each account via visit by field representative. The representative informed the account of the problem and removed the product.
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 noticeDistribution
As reported by FDA
CT, IL, IN, MD, MI, MS, NY, OK, PA, TN, WA
Page updated: Jan 10, 2026