TELEFLEX MEDICAL INC Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.
Brand
TELEFLEX MEDICAL INC
Lot Codes / Batch Numbers
Lot/Batch Numbers: 1811421 1812421 1901421 1904421 1905421 1906421 1907421 1908421 1909421
Products Sold
Lot/Batch Numbers: 1811421 1812421 1901421 1904421 1905421 1906421 1907421 1908421 1909421
TELEFLEX MEDICAL INC is recalling Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) - Product Usage: The laryngosco due to Breaking at the point of a welded joint. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Breaking at the point of a welded joint
Recommended Action
Per FDA guidance
Teleflex issued an Urgent Medical Device Recall on 07/06/2020. It states the following: 1. Immediately discontinue distribution and quarantine any products with the product code and lot number listed. 2. Using the provided customer letter and recall acknowledgement form templates, communicate this recall to any of your customers who have received product included within the scope of the recall. 3. Have the customers return any affected product to you, together with a completed Recall Acknowledgement Form, for consolidation and return to Teleflex Medical. In the event that an alternative approach is needed, contact Teleflex Medical Customer Service for more information at 1-866-396-2111. 4. To return recalled products to Teleflex Medical, complete the enclosed Recall Acknowledgement Form and fax it to 1-855-419-8507, Attn: Customer Service or email to recalls@teleflex.com. This will allow the firm to document the amount of product you have on hand for return. A customer service representative will contact you with a Return Goods Authorization (RGA) Number and will provide instructions for the return of product to Teleflex Medical. 5. Once you have completed returning all of the recalled products from your own inventory, and collecting and consolidating all of the recalled products from your customers, please check the box on the enclosed Recall Acknowledgment Form that indicates that you have completed the recall and fax it to 1-855-419-8507, Attn: Customer Service, or email it to recalls@teleflex.com. This will allow to document completion of the recall. 6. If you and your customers have no affected stock, please complete the enclosed Recall Acknowledgment Form and fax it to 1-855-419-8507, Attn: Customer Service or email to recalls@teleflex.com. This will allow to document your receipt of this letter. If you have any other questions,contact your local sales representative or Customer Service at 1-866-396-2111.
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 noticePage updated: Jan 10, 2026