Z-2279-2017Class II
AGB+ Pressure Injectable Multi-Lumen CVC Kit The Arrow Central Venous Catheters are intended to permit venous...
Arrow International LLC (subsidiary of Teleflex Incorporated) / initiated 2017-03-20 / Terminated / root cause: packaging
Arrow International Inc began a recall of AGB+ Pressure Injectable Multi-Lumen CVC Kit The Arrow Central Venous Catheters are intended to permit venous access to the central circulation by way of the... 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-2279-2017
- Classification
- Class II
- Status
- Terminated
- Initiated
- Posted
- Terminated
- Recalling firm
- Arrow International LLC (subsidiary of Teleflex Incorporated)
- Product
- AGB+ Pressure Injectable Multi-Lumen CVC Kit The Arrow Central Venous Catheters are intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins.The ARROWg+ard Blue Catheter permits venous access to the central circulation by way of the femoral, jugular, or subclavian veins. The ARROWg+ard technology is intended to provide protection against catheter-related bloodstream infections. It is not intended to be used as a treatment for existing infections nor is it indicated for long-term use (>30 days). The ARROWg+ard Blue PLUS Multiple-Lumen Catheter permits venous access to the central circulation by way of the femoral, jugular, or subclavian veins. The ARROWg+ard technology is intended to provide protection against catheter-related bloodstream infections (CRBSI). It is not intended to be used as a treatment for existing infections nor is it indicated for long-term use (>30 days). Clinical effectiveness of the ARROWg+ard Blue PLUS catheter in preventing CRBSI's compared to the original ARROWg+ard Blue catheter has not been studied
- 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.
- Distribution
- Nationwide Distribution
- Product codes and lots
- Material number CDA-42703-P1A
Enforcement reports
One row per recalled product line| Recall number | Class | Status | Voluntary or mandated | Report date | Classified |
|---|---|---|---|---|---|
| Z-2253-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2254-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2255-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2256-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2257-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2258-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2259-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2260-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2261-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2262-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2263-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2264-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2265-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2266-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2267-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2268-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2269-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2270-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2271-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2272-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2273-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2274-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2275-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2276-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2277-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2278-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2279-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2280-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2281-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2282-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2283-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2284-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2285-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2286-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2287-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2288-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2289-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2290-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2291-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2292-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2293-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2294-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2295-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2296-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2297-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2298-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2299-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2300-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2301-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2302-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2303-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2304-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2305-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2306-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2307-2017 | Class II | Terminated | Voluntary: Firm initiated | ||
| Z-2308-2017 | Class II | Terminated | Voluntary: Firm initiated |
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What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.