Karl Storz Endoscopy America Inc 600 Corporate Pointe Storz Documentation Cart with Articulating Arm, Model Number 9601F Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Storz Documentation Cart with Articulating Arm, Model Number 9601F
Brand
Karl Storz Endoscopy America Inc 600 Corporate Pointe
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Serial numbers: 82861-8 84504-21 84505-10 84505-30 84987-15 82859-4 82859-5 82859-6 82859-7 82858-8 82858-9 82858-10 81553-1 85358-35 80486C-9 84505-14 82861-1 82861-2 82861-3 82861-4 82861-5 80486C-17 81553-14 81553-20 84987-17 84987-18 84987-19 84987-20 84987-21 84987-22 84987-23 84987-24 84987-34 84987-35 84504-20 84504-24 85358-9 80485-1 80485-2 81552-11 81552-10 81553-19 85358-37 80486C-1 80486C-2 84505-12 82858-4 82858-5 82858-6 82858-7 84987-6 84987-7 84987-8 84987-9 84987-10 84987-11 84504-17 84504-18 84504-19 84505-19 84505-20 84505-21 84505-16 84505-17 84505-18 85358-41 84504-28 82859-3 82859-2 80486C-3 80486C-4 80486C-5 80486C-6 80486C-6 84504-9 84504-10 82861-10 82861-9 81553-6 81553-7 81552-37 81552-19 81552-18 84505-27 84505-28 85358-40 82861-7 82861-6 82860-1 84987-1 84987-2 84505-7 81553-18 81553-18 84987-3 84987-16 84504-26 85358-15 85358-16 85358-17 85358-18 85358-19 85358-20 85358-38 85358-39 85358-1 85358-2 85358-3 85358-4 85358-5 85358-6 80486C-8 85358-21 84505-24 84505-9 81552-14 81552-15 81552-16 80486C-14 81552-17 82860-2 82860-3 82860-4 82860-5 85358-33 85358-34 85358-48 85358-49 85358-50 84505-1 84505-2 84505-3 84505-4 85358-45 85358-46 85358-47 81552-22 81552-23 81552-24 81552-25 81552-26 81552-27 81552-28 81552-29 81552-30 81552-31 81552-32 81552-33 81552-34 81552-35 81553-8 81553-9 81552-4 81552-3 80485-7 82859-1 81553-3 81553-2 80486C-7 81553-10 81552-5 80486C-16 81552-6 80484B-16 80484B-17 80484B-18 80484B-19 80485-3 80485-4 82860-9 82858-1 80484B-6 80484B-7 80484B-8 80484B-9 80484B-10 80484B-11 80484B-12 80484B-13 80484B-14 80484B-15 84957A-1 84957A-3 84957A-5 84957A-4 84957A-7 84957A-2 84957A-6 84504-25 85358-8 85358-9 80486C-11 80486C-12 81553-13 82860-6 82860-7 82860-8 80485-8 80485-9 80485-10 84505-8 80484B-20 81553-4 81553-5 82858-3 85358-26 85358-27 85358-28 85358-29 85358-30 85358-31 85358-32 84987-5 84987-4 81553-15 81553-16 84505-15 85358-10 85358-11 85358-12 85358-13 84504-16 84505-22 84505-23 85358-42 85358-43 85358-44 84504-29 81552-13 80485-5 80485-6 84504-11 84504-12 84504-13 84504-14 84504-15 80486C-19 80486C-20 84505-13 84987-12 84987-28 84987-29 84987-30 84987-31 84987-32 84987-33 84987-3 84987-3 86058-1 86058-2 86058-3 86058-4 86058-5 86058-6 86058-7 86058-8 84987-25 84987-26 84987-27 84987-13 84987-14 86058-11 86058-10 86058-9 86058-12 86058-13 86058-14 86058-15 86747-1 86747-2 86747-3 86747-4 86747-5 86747-6 86747-7 86747-8 86747-9 86747-10 86058-18 86058-17 86747-12 86747-13 86747-14 86747-15 86747-16 86747-11 86747-17 86747-18 86747-29 86747-30 86747-28 86747-21 86747-22 86747-23 86747-24 86747-20 86747-27 86747-31 86747-32 86747-33 86747-34 86747-35 86747-39 86747-38 86747-37 86747-36 86747-49 86747-50 86747-48 86747-46 86747-47 86747-43 86747-44 86747-45 86747-42 86058-2 86058-3 84987-36 84987-37 86058-1 82859-9 82859-10 84504-1 84504-3 84504-4 84504-5 84504-6 84504-7 84504-8 84504-2
Karl Storz Endoscopy America Inc 600 Corporate Pointe is recalling Storz Documentation Cart with Articulating Arm, Model Number 9601F due to THE ARTICULATING ARM ON THE CART, WHICH HOLDS THE MONITOR, MAY FALL OFF FROM THE CART DURING MANIPULATION. WHEN IT FALLS, IT COULD HIT THE GROUND OR F. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
THE ARTICULATING ARM ON THE CART, WHICH HOLDS THE MONITOR, MAY FALL OFF FROM THE CART DURING MANIPULATION. WHEN IT FALLS, IT COULD HIT THE GROUND OR FALL ON THE PEOPLE/OBJECTS THAT ARE IN CLOSE PROXIMITY.
Recommended Action
Per FDA guidance
Alert letter mailed 03/10/2006 via FedEx to all direct accounts. The firm was instructed to complete the Customer Response Form, which included a box to be checked for who will do the correction (The Customer or The Firm), and fax it back. After the correction is completed, the firm is to fax the Customer Response form a second time completing part 2 of the form.
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