Teleflex Medical Hudson RICA Sheridan, Sher-I-Bronch Accessory Pack, Teleflex Medical, Research Triangle Park, NC 27709. Indicated for use in thoracic surgery, bronchospirometry, for the administration of endobronchial anesthesia and other uses commonly associated with endobronchial tubes. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Hudson RICA Sheridan, Sher-I-Bronch Accessory Pack, Teleflex Medical, Research Triangle Park, NC 27709. Indicated for use in thoracic surgery, bronchospirometry, for the administration of endobronchial anesthesia and other uses commonly associated with endobronchial tubes.
Brand
Teleflex Medical
Lot Codes / Batch Numbers
Catalog Number: 5-16142, Lot Numbers: 1162530, 1167118, 1169739, 1169740, 1190331, 1200165 and 1207348.
Products Sold
Catalog Number: 5-16142, Lot Numbers: 1162530, 1167118, 1169739, 1169740, 1190331, 1200165 and 1207348.
Teleflex Medical is recalling Hudson RICA Sheridan, Sher-I-Bronch Accessory Pack, Teleflex Medical, Research Triangle Park, NC 277 due to The tether attaching to the double swivel cap may partially or completely break at the attachment points, resulting in the potential of the accidental. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The tether attaching to the double swivel cap may partially or completely break at the attachment points, resulting in the potential of the accidental aspiration of the tether into the patient's lungs.
Recommended Action
Per FDA guidance
Teleflex Medical, Inc. notified consignees via overnight mail starting July 31, 2009 requesting acknowledgement of the recall and a request to return all of the affected product. Distributors were instructed to forward the letter to their consignees and retrieve relevant product from those locations. Affected product received by Teleflex Medical will be destroyed or reworked and replacement product or credit will be provided to the consignee. For further information, contact Teleflex Medical at 1-919-433-4986.
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