Recall Z-0730-2024
Oakworks Inc · initiated December 5, 2023
Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature
Product
Ultrasound EA (Ergonomic Advantage) table version; V2 (Vascular 2 Section) Echocardiography -An Ultrasound examination table
Codes / lots: (UDI): 00817463025521 S/N: VCF805597 VCF814488 VCF814750 VCF817222 VCF817223 VCF817720 VCF817721 VCF823450 VCF825629 VCF825630 VCF833350 VCF813968 VCF817520 VCF826533 VCF822117 VCF824501 VCF824502 VCF824503 VCF824504 VCF815120 VCF814849 VCF835728
Reason for recall
Backrest platform stress fracture - the table is not operational in an inclined position
FDA-determined cause: Device Design
Action taken
Oakworks Inc. issued "URGENT: MEDICAL DEVICE RECALL/CORRECTION" letter on 12/5/23 via Certified Mail/Email to Distributors and End Users. Letter states reason for recall, health risk and action to take: 1. Immediately examine your inventory of OAKWORKS Inc. Ultrasound EA Table with Echocardiography, or Electric Access Back Supports [left & right] to identify and locate all affected product(s). 2. For tables in use, they remain fully functional if the backrest platform stress fracture has not occurred. For tables that have the stress fracture or break, only use in a flat position until the backrest is replaced. 3. Implement the field action as described below for the product listed in the Product and Distribution Information Table. 4. Enclosed is a Medical Device Advisory Notice Response Form for each product we believe you have. Please complete this form in its entirety and return to OAKWORKS Inc., within 48 hours of receipt of this advisory notice via any of the options listed below. MAIL: Oakworks Inc. EMAIL: customerservice@oakworks.com Attn: Customer Service MDAN Response 923 East Wellspring Rd. New Freedom, PA 17349 Action by OAKWORKS Inc.: Upon receipt of the Medical Device Advisory Notice Response Form(s), and to minimize the downtime of your OAKWORKS Ultrasound EA table, we will setup a service visit to replace the backrest (if a stress fracture has occurred) or install a reinforcement plate (if a stress fracture has not occurred) on the table(s). The correction installation takes approximately 30 minutes. The replaced backrest will be disposed of by the service provider. Additional Information: If you have any questions or concerns, please contact our Customer Service Department at 800-558-8850 or 717-235-6807 Monday through Friday, 8:00 AM to 5:00 PM, Eastern Time.
Details
- Recall number
- Z-0730-2024
- Initiated
- December 5, 2023
- Posted by FDA
- January 13, 2024
- Product code
- LGX – Table, Examination, Medical, Powered
- Quantity
- 28 units
- Distribution
- US Nationwide Distribution
- Recalling firm
- Oakworks Inc, New Freedom, PA
Other products in the same recall event
| Recall | Product | Initiated |
|---|---|---|
| Z-0727-2024 Class II | Ultrasound EA (Ergonomic Advantage) table versions; G2 (GENERAL 2) -An Ultrasound…Backrest platform stress fracture - the table is not operational in an inclined position | 12/05/2023Open, Classified |
| Z-0728-2024 Class II | Ultrasound EA (Ergonomic Advantage) table versions; G3 (General 3 Section)…Backrest platform stress fracture - the table is not operational in an inclined position | 12/05/2023Open, Classified |
| Z-0729-2024 Class II | Ultrasound EA (Ergonomic Advantage) table versions; G3 Multi-Specialty Echocardiography…Backrest platform stress fracture - the table is not operational in an inclined position | 12/05/2023Open, Classified |