USA Instruments Incorporated The recalled product is the Disposable biopsy plate, part #U1-150131. The biopsy plate is labeled in part: Disposable Biopsy Plate, part U1-150131, 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 and with OEM coils (coils manufactured for Philips and Hitachi by USA Instruments) during Magnetic Resonance breast biopsy procedures. The disposable biopsy plate for use with GE coils is packaged and sold as Recall
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According to the U.S. Food and Drug Administration (FDA)
Product
The recalled product is the Disposable biopsy plate, part #U1-150131. The biopsy plate is labeled in part: Disposable Biopsy Plate, part U1-150131, 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 and with OEM coils (coils manufactured for Philips and Hitachi by USA Instruments) during Magnetic Resonance breast biopsy procedures. The disposable biopsy plate for use with GE coils is packaged and sold as
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USA Instruments Incorporated
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USA Instruments Incorporated is recalling The recalled product is the Disposable biopsy plate, part #U1-150131. The biopsy plate is labeled in 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
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Page updated: Jan 10, 2026