Teleflex Medical Conditional Fiber Optic Laryngoscope Kit, which contains laryngoscope blades, handles and 2 battery packs for use in Magnetic Resonance environments; Distributed by Teleflex Medical, Research Triangle Park, NC 27709; catalog number 005852300 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Conditional Fiber Optic Laryngoscope Kit, which contains laryngoscope blades, handles and 2 battery packs for use in Magnetic Resonance environments; Distributed by Teleflex Medical, Research Triangle Park, NC 27709; catalog number 005852300
Brand
Teleflex Medical
Lot Codes / Batch Numbers
catalog number 005852300, battery lot numbers 065201-065228, 065231, 065232, 065233
Products Sold
catalog number 005852300, battery lot numbers 065201-065228, 065231, 065232, 065233
Teleflex Medical is recalling Conditional Fiber Optic Laryngoscope Kit, which contains laryngoscope blades, handles and 2 battery due to The MRI Battery is out of specification for its magnetic content.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The MRI Battery is out of specification for its magnetic content.
Recommended Action
Per FDA guidance
Teleflex telephoned the account on 3/1/07, and faxed them a follow-up recall letter on the same date. The account was informed that the batteries did not meet specification, and was requested to check the batteries in the laryngoscope kit shipped to them for the affected battery lot numbers, and return the affected batteries to Teleflex for replacement. Any questions were directed to Linda Todd at 1-800-334-9751, ext. 4951.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
GA
Page updated: Jan 10, 2026