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-2283-2017Class II

Arrow VPS Access Kit with Maximal Barrier Precautions for use with 4 Fr. Peripherally Inserted Central Venous...

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

Arrow International Inc began a recall of Arrow VPS Access Kit with Maximal Barrier Precautions for use with 4 Fr. Peripherally Inserted Central Venous Catheter The intended use of the VPS Stylet and... 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-2283-2017
Classification
Class II
Status
Terminated
Initiated
Posted
Terminated
Recalling firm
Arrow International LLC (subsidiary of Teleflex Incorporated)
Product
Arrow VPS Access Kit with Maximal Barrier Precautions for use with 4 Fr. Peripherally Inserted Central Venous Catheter The intended use of the VPS Stylet and Console (VPS System) is to quickly and accurately guide market available peripherally inserted central catheters (PICCs) to the goal location which is to the cavo-atrial junction near the sino-atrial node
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
unknown-firm reports total devices distributed 43,394
Distribution
Nationwide Distribution
Product codes and lots
Material number ASK-04001-DU8

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-2283-2017
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