510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-2261-2017Class II

Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath, Integral Hemostatis Valve/Side Port...

Arrow International LLC (subsidiary of Teleflex Incorporated) / initiated 2017-03-20 / Terminated / root cause: packaging

Arrow International Inc began a recall of Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath, Integral Hemostatis Valve/Side Port, Sharps Safety Features and Maximal Barrier Precautions... on . FDA classified it as Class II and gives the reason as "Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products". As of , the recall status on record is Terminated, and MDM tags the root cause as packaging.

Recall record

Recall number
Z-2261-2017
Classification
Class II
Status
Terminated
Initiated
Posted
Terminated
Recalling firm
Arrow International LLC (subsidiary of Teleflex Incorporated)
Product
Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath, Integral Hemostatis Valve/Side Port, Sharps Safety Features and Maximal Barrier Precautions for use with 7.5-8 Fr. Catheters. The Arrow Percutaneous Sheath Introducer permits venous access and catheter introduction to the central circulation. The ARROWg+ard antimicrobial surface is intended to help provide protection against sheath-related infections. The sheath is not intended to be used as a treatment for existing infections, nor is it indicated for long-term use
Product code
FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Reason for recall
Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.
Root cause tag
packaging
FDA root cause
Under Investigation by firm
Action
Arrow International sent an Urgent Medical Device Notification Letter dated April 5, 2017, to affected customers to inform them of the issue. The notice provided safety instructions for using the product and instructed customers to return the enclosed acknowledgement form indicating the notice was received, and fax it to 855-419-8507, Attn: Customer Service or email to [email protected]. Customers with questions were instructed to call 1-866-246-6990. For questions regarding this recall call 610-378-0131.
Quantity in commerce
43,394 units
Distribution
Nationwide Distribution
Product codes and lots
Material Number ASK-29803-MM

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-2261-2017
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-2253-2017Class IITerminatedVoluntary: Firm initiated
Z-2254-2017Class IITerminatedVoluntary: Firm initiated
Z-2255-2017Class IITerminatedVoluntary: Firm initiated
Z-2256-2017Class IITerminatedVoluntary: Firm initiated
Z-2257-2017Class IITerminatedVoluntary: Firm initiated
Z-2258-2017Class IITerminatedVoluntary: Firm initiated
Z-2259-2017Class IITerminatedVoluntary: Firm initiated
Z-2260-2017Class IITerminatedVoluntary: Firm initiated
Z-2261-2017Class IITerminatedVoluntary: Firm initiated
Z-2262-2017Class IITerminatedVoluntary: Firm initiated
Z-2263-2017Class IITerminatedVoluntary: Firm initiated
Z-2264-2017Class IITerminatedVoluntary: Firm initiated
Z-2265-2017Class IITerminatedVoluntary: Firm initiated
Z-2266-2017Class IITerminatedVoluntary: Firm initiated
Z-2267-2017Class IITerminatedVoluntary: Firm initiated
Z-2268-2017Class IITerminatedVoluntary: Firm initiated
Z-2269-2017Class IITerminatedVoluntary: Firm initiated
Z-2270-2017Class IITerminatedVoluntary: Firm initiated
Z-2271-2017Class IITerminatedVoluntary: Firm initiated
Z-2272-2017Class IITerminatedVoluntary: Firm initiated
Z-2273-2017Class IITerminatedVoluntary: Firm initiated
Z-2274-2017Class IITerminatedVoluntary: Firm initiated
Z-2275-2017Class IITerminatedVoluntary: Firm initiated
Z-2276-2017Class IITerminatedVoluntary: Firm initiated
Z-2277-2017Class IITerminatedVoluntary: Firm initiated
Z-2278-2017Class IITerminatedVoluntary: Firm initiated
Z-2279-2017Class IITerminatedVoluntary: Firm initiated
Z-2280-2017Class IITerminatedVoluntary: Firm initiated
Z-2281-2017Class IITerminatedVoluntary: Firm initiated
Z-2282-2017Class IITerminatedVoluntary: Firm initiated
Z-2283-2017Class IITerminatedVoluntary: Firm initiated
Z-2284-2017Class IITerminatedVoluntary: Firm initiated
Z-2285-2017Class IITerminatedVoluntary: Firm initiated
Z-2286-2017Class IITerminatedVoluntary: Firm initiated
Z-2287-2017Class IITerminatedVoluntary: Firm initiated
Z-2288-2017Class IITerminatedVoluntary: Firm initiated
Z-2289-2017Class IITerminatedVoluntary: Firm initiated
Z-2290-2017Class IITerminatedVoluntary: Firm initiated
Z-2291-2017Class IITerminatedVoluntary: Firm initiated
Z-2292-2017Class IITerminatedVoluntary: Firm initiated
Z-2293-2017Class IITerminatedVoluntary: Firm initiated
Z-2294-2017Class IITerminatedVoluntary: Firm initiated
Z-2295-2017Class IITerminatedVoluntary: Firm initiated
Z-2296-2017Class IITerminatedVoluntary: Firm initiated
Z-2297-2017Class IITerminatedVoluntary: Firm initiated
Z-2298-2017Class IITerminatedVoluntary: Firm initiated
Z-2299-2017Class IITerminatedVoluntary: Firm initiated
Z-2300-2017Class IITerminatedVoluntary: Firm initiated
Z-2301-2017Class IITerminatedVoluntary: Firm initiated
Z-2302-2017Class IITerminatedVoluntary: Firm initiated
Z-2303-2017Class IITerminatedVoluntary: Firm initiated
Z-2304-2017Class IITerminatedVoluntary: Firm initiated
Z-2305-2017Class IITerminatedVoluntary: Firm initiated
Z-2306-2017Class IITerminatedVoluntary: Firm initiated
Z-2307-2017Class IITerminatedVoluntary: Firm initiated
Z-2308-2017Class IITerminatedVoluntary: Firm initiated