FDA Medical Device Recalls (openFDA)
Karl Storz Endoscopy America Inc: Storz Documentation Cart with Articulating Arm, Model Number 9601F
- Recall number
- Z-0769-06
- Recalling firm
- Karl Storz Endoscopy America Inc
- Product
- Storz Documentation Cart with Articulating Arm, Model Number 9601F
- Status
- Terminated
- Initiated
- 2006-03-10
- Posted
- 2006-04-19
- Terminated
- 2008-08-07
- Reason
- 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.
- Root cause
- Process control
- Action
- 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.
- Quantity
- 333
- Distribution
- NATIONWIDE
- Lot, serial or model codes
- 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
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- KOG
- Firm FEI
- 2020550
- Firm city
- Culver City
- Firm state
- CA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28