Reported Oct 22, 2014 · Terminated

Arrow Select Kits (ASK) and Maximal Barrier Precautions Kits (CDC) with BD Medical Posiflush 10mL Saline Flush Syringe.

Arrow International Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Arrow International Inc · 2400 Bernville Rd · Reading, PA · 19605-9607

Is this the product you have?

Arrow Select Kits (ASK) and Maximal Barrier Precautions Kits (CDC) with BD Medical Posiflush 10mL Saline Flush Syringe.

Lot codes and dates: Product Numbers
101 of 101 codes
ASK-04001-VCUH
ASK-04510-MM3
ASK-05001-TSC
ASK-05052-QV
ASK-05052-SFL
ASK-05502-UWMC
ASK-05541-MS2
ASK-09804-SPH
ASK-09810-PCMH1
ASK-09903-ECL
ASK-09903-PCMH1
ASK-11142-MGH3
ASK-12703-MGH2
ASK-12703-SPH
ASK-15703-MH
ASK-15854-FAM ASK-17702-PJHH1
ASK-21142-HF2
ASK-21242-PCMH1
ASK-21242-SFM1
ASK-21242-UVA3
ASK-29803-HF3
ASK-29803-MM
ASK-29803-MS
ASK-29903-UK
ASK-29903-UK
ASK-34041-PTG
ASK-34052-PTG
ASK-35052-PTG
ASK-42703-AMC
ASK-42703-OHU1
ASK-42703-PCCH1
ASK-42703-PCSJ
ASK-42703-PPMC
ASK-42703-PSBM
ASK-42703-PSCH
ASK-42703-PSFM
ASK-42703-PTRH
ASK-42703-SJMT
ASK-42703-UHC
ASK-42802-ECL1
ASK-42802-PMCG
ASK-42802-PUCS
ASK-42854-CMC2
ASK-45703-MM2
ASK-45703-NYU1
ASK-45703-PCCH1
ASK-45703-PCHS1
ASK-45703-PCSJ
ASK-45703-PDCH
ASK-45703-PGBM1
ASK-45703-PHCH
ASK-45703-PHF
ASK-45703-PHF1
ASK-45703-PHPA2
ASK-45703-PIA
ASK-45703-PLGH1
ASK-45703-PMHG
ASK-45703-PSA
ASK-45703-PTMC
ASK-45703-PUAB
with lot numbers
145 of 145 codes
23F13H1030
23F13H0046
RF3053077
23F13J0406
23F13H0230
23F13J0435
23F13J0440
23F13H1031
23F13J0181
23F13G0409
23F13H0060
23F13H0231
RF3053088
23F13H0232
23F13H0062
23F13H0233
RF3053092
RF3053096
23F13J0072
23F13H0520
23F13H1032
23F13H0064
23F13J0446
23F13H0804
23F13J0187
23F13H0069
23F13J0193
23F13H1033
23F13G0724
23F13H0898
RF3053035
23F13J0202
23F13H0297
RF3053111
23F13H0521
23F13G0402
23F13G0404
23F13H1034
23F13G0495
23F13J0399
23F13H0072
23F13H0808
23F13H0810
23F13H0313
RF3053655
23F13J0208
23F13H0315
23F13H0768
23F13J0254
RF3052973
23F13J0204
23F13J0037
23F13J0352
23F13J0207
23F13H0687
23F13H0512
23F13J0349
23F13J0452
RF3040503
23F13G0472
Amount recalled: 71255

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Multi-Lumen Central Venous Catheterization Kit

Where it was sold

Nationwide

Why it was recalled

The component supplier recalled their 0.9% Sodium Chloride Injection USP BD Posiflush SF Saline Flush Syringe 10mL because some unit packages may exhibit open seals which impact package integrity and potentially product sterility.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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