Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets recall: Labeling Error
Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets manufactured from galvanized carbon steel and aluminum rods that are…
Why was Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets recalled?
Product size listed on the labeling is incorrect.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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 5-15103 - Lot Number 73J1600218, 73K1600376, 73K1600587, 73L1600158, 73M1600275, 73A1700733;
- Product
- Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets manufactured from galvanized carbon steel and aluminum rods that are…
- Recalling firm
- Teleflex Medical
- Quantity
- 21,690 eaches
- Distribution
- Worldwide Distribution - US Nationwide in the states of CT, FL, ID, IN, KY, MA, MI, MN, MO, NE, NJ, NY, NC, OH, PA, RI, SD, TX, UT, WA and countries of Canada, Czech Republic, Denmark, Germany, Israel, & Portugal
- Recall date
- June 21, 2017
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)