Drug recall

Palindrome HSI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 19cm Item Code: 8888145048

FDA recall event 70985 · Class II · Covidien LLC

Key facts

Event ID 70985
Recall numbers Z-1850-2015, Z-1851-2015, Z-1852-2015, Z-1853-2015, Z-1854-2015, Z1855-2015, Z1856-2015, Z-1857-2015, Z-1858-2015, Z-1859-2015, Z-1860-2015, Z-1861-2015 and 50 more
Recalling firm Covidien LLC
Product type Devices
Products Palindrome HSI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 19cm Item Code: 8888145048, Palindrome HSI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 19cm Item Code: 8888145057C, Palindrome HSI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 23cm Item Code: 8888145048C, Palindrome HSI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 28cm Item Code: 8888145049, Palindrome HSI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 28cm Item Code:8888145049C and 51 more
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Catheters may not meet antimicrobial specification
Initiation date Apr 23, 2015
Report date Jul 8, 2015
Termination date Jul 26, 2017
City North Haven
State CT
Country United States
FEI number 1219930

At a glance

  • 10–99 Products in this recall
  • 10–99 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date:

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