King LT-D Oropharyngeal Airways The King LT-D is recall
King LT-D Oropharyngeal Airways The King LT-D is intended for use in adult patients (in excess of 25 kg) for controlled ventilation during anesthesia…
Why was King LT-D Oropharyngeal Airways The King LT-D is recalled?
Report that size 5 KLTD airways were packaged in pouches indicating a size of 2.5 and shipped to your facility. The correct size of the KLTD airway is clearly marked on the actual airway product and the physical size difference between 2.5 and 5 is distinct and obvious.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Part Number KLTD2125 Lot Number I10RG
- Product
- King LT-D Oropharyngeal Airways The King LT-D is intended for use in adult patients (in excess of 25 kg) for controlled ventilation during anesthesia…
- Recalling firm
- King Systems Corp.
- Quantity
- 9 cases; 45 products
- Distribution
- Distributed in NY.
- Recall date
- September 25, 2013
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)