TELEFLEX MEDICAL INC Recall 87370
Description: RUSCH¿ POLARIS" Laryngoscope - Product Usage: intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.
TELEFLEX MEDICAL INC Recall 87370 Information
Status | Ongoing |
Mandated? | Voluntary: Firm initiated |
Recall Number | Z-1294-2021 |
Event ID | 87370 |
Event Description | RUSCH¿ POLARIS" Laryngoscope - Product Usage: intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation. |
Product Type | Devices |
Distribution | Worldwide distribution - US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI. The country of Canada. |
Quantity | 157, 150 units (156,980 units in the US; 170 units OUS) |
Recall Reason | Teleflex is voluntarily recalling the products referenced above due to customers reporting that the laryngoscope handles develop cracks and/or break at the hinge. |
Device Classification | 20210331 |
Device Code Info | Model 44401 (GTIN: Each: 14026704662552 Box: 24026704662559 Case: 34026704662556; lots 197, 19A, 19F, 19J, 19P, 19W, 205, 207, 20C, 20H, 20T); Model 44402 (GTIN: Each: 14026704662569 Box: 24026704662566 Case: 34026704662563; lots 197, 19A, 19F, 19J, 19P, 19W, 205, 207, 20C, 20H, 20M, 20T); Model 44403 (GTIN: Each: 14026704662576 Box: 24026704662573 Case: 34026704662570; lots 197, 19A, 19F, 19J, 207, 20C, 20H, 20M, 20T). |
Center Classification Date | 20210323 |
Recall Initiation Date | 20210218 |
Recalling Firm | TELEFLEX MEDICAL INC |
Initial Notification | Letter |
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