Emerald Fiberoptic Blade recall: Labeling Error
Emerald Fiberoptic Blade, Macintosh 4, Teleflex Medical. A rigid laryngoscope is a device used to examine and visualize a patient's upper airway and…
Why was Emerald Fiberoptic Blade recalled?
Packaging Error: Customers have reported receiving incorrect product. The box labeling indicates the correct product MAC 4 but the contents are incorrect, Miller 4 blades.
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?
Product Code: 004434400, Lot number: 02A1402138
- Product
- Emerald Fiberoptic Blade, Macintosh 4, Teleflex Medical. A rigid laryngoscope is a device used to examine and visualize a patient's upper airway and…
- Recalling firm
- Teleflex Medical
- Quantity
- 120 units
- Distribution
- US Distribution including the states of FL, GA, KY, MD, MS, MT, PA, SC and TX.
- Recall date
- August 6, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)