Recall Z-2587-2017— Teleflex Medical
Class II · Ongoing
Class II FDA medical device recall by Teleflex Medical, initiated 2017-05-11. FDA's recall record names no specific 510(k) clearance for this event. Product: Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets manufactured from galvanized carbon steel and aluminum rods that are coated with a blue PVC or polypropylene outer covering and are designed to be placed inside an endotracheal tube to obtain a desired shape during intubation.. Reason: Product size listed on the labeling is incorrect..
- Recalling firm
- Teleflex Medical
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2017-05-11
- Firm location
- Research Triangle Park, NC, United States
Product description
Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets manufactured from galvanized carbon steel and aluminum rods that are coated with a blue PVC or polypropylene outer covering and are designed to be placed inside an endotracheal tube to obtain a desired shape during intubation.
Reason for recall
Product size listed on the labeling is incorrect.
Data sourced from openFDA. This site is unofficial and independent of the FDA.