Spiegelberg Gmbh & Co. KG Tempowerkring 4 Hamburg Germany Spiegelberg Brain Pressure Monitoring System Probe 3PN, REF: SNDI3.1.531FV534P and Probe 3PS, REF: SNDI3.1.63/FV535P Product Usage: lntracranial pressure measuring probes are used to measure intracranial pressure (intracranial pressure, ICP), so the pressure in the head. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Spiegelberg Brain Pressure Monitoring System Probe 3PN, REF: SNDI3.1.531FV534P and Probe 3PS, REF: SNDI3.1.63/FV535P Product Usage: lntracranial pressure measuring probes are used to measure intracranial pressure (intracranial pressure, ICP), so the pressure in the head.
Brand
Spiegelberg Gmbh & Co. KG Tempowerkring 4 Hamburg Germany
Lot Codes / Batch Numbers
Probe 3PN SND1 3.1 .53/FV534P: SNs: 12835-1 3393, Probe 3PS SND13.1 .63/FV535P: SNs: 6937-7122
Products Sold
Probe 3PN SND1 3.1 .53/FV534P: SNs: 12835-1 3393; Probe 3PS SND13.1 .63/FV535P: SNs: 6937-7122
Spiegelberg Gmbh & Co. KG Tempowerkring 4 Hamburg Germany is recalling Spiegelberg Brain Pressure Monitoring System Probe 3PN, REF: SNDI3.1.531FV534P and Probe 3PS, REF: S due to In the vast majority of products specified, a shrinkage of the air chamber during sterilization has occurred. Because of these false high readings wer. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
In the vast majority of products specified, a shrinkage of the air chamber during sterilization has occurred. Because of these false high readings were displayed in the lower measuring range from 0 to 20 mmHg. The observed measurement error was particularly at the lowest end of the range (to 0 mmHg) up to 8 mmHg.
Recommended Action
Per FDA guidance
Spiegelberg Gmbh & Co. KG sent an Urgent Medical Device Recall letter dated December 29, 2009, to all affected customers. Customers were instructed to quarantine and return stored products. Furthermore, they were asked to inform all their customers which have received the affected products and recall the products accordingly. Furthermore, they were asked to tell us about the actions taken by them.
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