Silicone CTS (Close to Shaft) Cuff Adjustable Neck Flange Tracheostomy Tube (Wire Reinforced), Arcadia Medical Silicone
FDA device recall Z-2657-2011 · posted 2011-06-24 · Terminated
Recall details
- Recalling firm
- Arcadia Medical Corporation
- Reason for recall
- The product does not contain a punched hole above the cuff access port (a lumen that enables suctioning of secretions proximal to the inflated cuff) as intended by the devices design. This eliminates the user's ability to suction secretions through this suction port, necessitating that the user revert to standard of care methods for suctioning secretions from around the cuffed trach tube shaft.
- Action taken
- Arcadia Medical Corporation sent a "MEDICAL DEVICE RECALL" letter on May 9, 2011 and email on May 8, 2011 to all affected costumers. The letter included; description of the product name, afffected lot numbers, description of the problem, instructions to discontinue use of the recalled devices and to return them to Arcadia Medical for replacement . The letter instructed the customers to email Arcadia Medical with the number of devices in their inventory. For additional information contact Arcadia Medical Corporation at 219-779-9431.
- Root cause
- Process control
- Status
- Terminated
- Product code
- BTO
- Quantity affected
- 118
- Distribution
- Worldwide Distribution --USA including the state of Ohio, and the countries of Denmark, Italy, Germany, Turkey, Slovakia, Isreal, France, Sweden, and Romania
- Date initiated
- 2011-05-08
- Date posted
- 2011-06-24
- Date terminated
- 2011-08-30
- Location
- Crown Point, IN
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| SILICONE FOAM CUFF TRACHEOSTOMY TUBES, SILICONE CUFFLESS NEONATAL AND PEDIATRIC TRACHEOSTOMY TUBES (K031553) | Arcadia Medical Corporation | 2003-11-18 |