USA Instruments Incorporated The recalled product is the Lateral biopsy plate, part #2414346. The biopsy plate is labeled in part: Lateral Biopsy Plate, part 2414346, For Use with the Liberty 9000 8-Channel Breast Coil, USA Instruments, Inc., Aurora, OH, sterile. The breast biopsy plate is used with GE coils during Magnetic Resonance breast biopsy procedures. The lateral biopsy plate is packaged and sold as a part of catalogue E8800BG, M3087JG, G3087JH, M3335LA. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
The recalled product is the Lateral biopsy plate, part #2414346. The biopsy plate is labeled in part: Lateral Biopsy Plate, part 2414346, For Use with the Liberty 9000 8-Channel Breast Coil, USA Instruments, Inc., Aurora, OH, sterile. The breast biopsy plate is used with GE coils during Magnetic Resonance breast biopsy procedures. The lateral biopsy plate is packaged and sold as a part of catalogue E8800BG, M3087JG, G3087JH, M3335LA.
Brand
USA Instruments Incorporated
Lot Codes / Batch Numbers
All lot codes.
Products Sold
All lot codes.
USA Instruments Incorporated is recalling The recalled product is the Lateral biopsy plate, part #2414346. The biopsy plate is labeled in part due to The packaging used for the Breast Biopsy plate may exhibit small holes or tears. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The packaging used for the Breast Biopsy plate may exhibit small holes or tears
Recommended Action
Per FDA guidance
The recalling firm notified consignees via certified letter, dated 1/31/07.
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
PR
Page updated: Jan 10, 2026