Sanarus Medical Inc Sanarus brand Centrica Rotational Core Biopsy medical device, Model/Product Code: CD-0500 (single Device); CD-1000 (5 pack) Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Sanarus brand Centrica Rotational Core Biopsy medical device, Model/Product Code: CD-0500 (single Device); CD-1000 (5 pack)
Brand
Sanarus Medical Inc
Lot Codes / Batch Numbers
Lot #: 28090403, 03-0085, 03-0086, C030401
Products Sold
Lot #: 28090403, 03-0085, 03-0086, C030401
Sanarus Medical Inc is recalling Sanarus brand Centrica Rotational Core Biopsy medical device, Model/Product Code: CD-0500 (single De due to Recent 'pre-tests' show that Argon gas has the potential to escape from the device during a biopsy procedure.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Recent 'pre-tests' show that Argon gas has the potential to escape from the device during a biopsy procedure.
Recommended Action
Per FDA guidance
On 5/13/03, the firm issued letters via Federal Express to all its direct consignees, informing them of the affected devices and providing instructions on the recall.
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
IL, MD, OH, OR, TN, TX
Page updated: Jan 10, 2026