Reported Jun 24, 2026 · Ongoing

Description/REF: RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-1A; RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-X1A; ARTERIAL CATHETER…

Arrow International, LLC

High riskUsing this product could cause serious injury, illness or death — stop using it now.

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, LLC · 3015 Carrington Mill Blvd · Morrisville, NC · 27560-5437

Is this the product you have?

37 of 37 products

Products covered by this recall
#Product as published
1Description/REF: RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-1A
2RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-X1A
3ARTERIAL CATHETER KIT: 18 GA X 16 CM/ASK-04018-HCA
4ARTERIAL CATHETER KIT: 18 GA X 16 CM/ASK-04018-UPM
5RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-HC
6ARTERIAL LINE KIT: 20 GA X 5IN (12 CM)/ASK-04020-HMC
7RADIAL ARTERY CATHETER KIT: 20 GA X 30MM/ASK-04020-MMC
8RA CATH KIT: 20 GA X 1-1/2IN (3.81 CM)/ASK-04020-SV
9ARTERIAL CATH KIT: 20 GA X 5 IN (12 CM)/ASK-04100-AMC-S1
10ARTERIAL CATHETER KIT: 20 GA X 12 CM/ASK-04100-NS
11RADIAL ARTERY KIT/ASK-04500-AH
12RAD ART:20GAX3.81CM / ART LINE:20GAX12CM/ASK-04500-HF-S
13ARTERIAL LINE KIT: 1L 20 GA X 12 CM/ASK-04510-HA
14ARTERIAL LINE KIT: 20 GA. X 5 IN (12 CM)/ASK-04510-HF
15ARTERIAL LINE KIT: 20 GA X 5 IN (12 CM)/ASK-04510-IHC1
16ARTERIAL LINE KIT: 20 GA X 5 IN (12 CM)/ASK-04510-MSK2
17ARTERIAL CATH KIT: 20GA X 5IN/ASK-04510-NS
18ARTERIAL CATHETER KIT: 20 GA X 12 CM/FS-04510-S
19ARTERIAL LINE KIT/HF-04510-1
20RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-BSM
Lot codes and dates

37 of 37 products

Products covered by this recall
#BarcodesProduct as published
110801902193275NA-04220-1A/10801902193275/33F26B0027
210801902193275NA-04220-X1A/10801902193275/33F24G0553, 33F25E0272, 33F25E1053, 33F25H0760, 33F25J0636
310801902119268ASK-04018-HCA/10801902119268/33F24A0078
45080190211764410801902193275ASK-04018-UPM/50801902117644, 10801902193275/33F23B0953, 33F24A0389, 33F24B0140, 33F24D0028, 33F24H0480, 33F24J0550, 33F24K0164, 33F25A0505, 33F25C0742, 33F25C0792, 33F25E0961, 33F25E1070, 33F25E1071, 33F25E1072, 33F25G0105, 33F25H0062, 33F25J0866, 33F25L0353, 33F26B0507
51080190212138410801902193275ASK-04020-HC/10801902121384, 10801902193275/33F24A0828, 33F24B0246, 33F24C0148, 33F24D0113, 33F24G0409, 33F24J0559, 33F24K0172, 33F24L0693, 33F25C0136, 33F25C0933, 33F25E0128, 33F25H0070, 33F25L0356
61080190211769110801902193275ASK-04020-HMC/10801902117691, 10801902193275/33F24A0324, 33F24A0743, 33F24B0248, 33F24C0150, 33F24D0115, 33F24H0475, 33F24K0174, 33F24L0802, 33F25H0072, 33F25J0872, 33F25L0395, 33F26B0650, 33S24A0743, 33S24C0150, 33F26B0673
71080190211776910801902193275ASK-04020-MMC/10801902117769, 10801902193275/33F24C0160, 33F24D0123, 33F24E0423, 33F24G0420, 33F24H0487, 33F24J0571, 33F24K0183, 33F24L0692, 33F25A0523, 33F25C0974, 33F25E0139, 33F25H0081, 33F25J0880, 33F25L0346, 33F25M0853
81080190211783710801902117837ASK-04020-SV/10801902117837, 10801902117837/33F24A0868, 33F24B0269, 33F24E0436, 33F24E0437, 33F24L0746, 33F25H0087, 33F25J0885, 33F26B0512
91080190212492710801902193275ASK-04100-AMC-S1/10801902124927, 10801902193275/33F24D0139, 33F24E0446, 33F24G0439, 33F24K0199, 33F25A0532, 33F25E0153, 33F25G0116, 33F25H0093, 33F25J0516, 33F26B0656
101080190219327510801902117929ASK-04100-NS/10801902193275, 10801902117929/33F24G0440, 33F24L0579, 33F24M0266, 33F25A0533, 33F25C0151, 33F25C0788, 33F25E0155, 33F25H0095, 33F25J0518, 33F25K0256, 33F25L0448, 33F25M0945, 33F26B0649, 33F26B0667
111080190211404110801902193275ASK-04500-AH/10801902114041, 10801902193275/33F24A0153, 33F24A0803, 33F24B0282, 33F24C0181, 33F24E0452, 33F24G0444, 33F24J0586, 33F25A0538, 33F25H0101, 33F25J0893
121080190211800110801902193275ASK-04500-HF-S/10801902118001, 10801902193275/33F24A0141, 33F24A0753, 33F24A1157, 33F24B0283, 33F24C0182, 33F24D0143, 33F24E0453, 33F24G0445, 33F24J0587, 33F24K0206, 33F24L0766, 33F25C0154, 33F25C0966, 33F25E0161, 33F25H0102, 33F25J0894, 33F25L0492, 33R25C0966
1310801902193275ASK-04510-HA/10801902193275/33F24J0591, 33F24K0210, 33F25B0685, 33F25C0911, 33F25E0166, 33F25E0993, 33F25J0524, 33F25L0449
141080190219327510801902118025ASK-04510-HF/10801902193275, 10801902118025/33F24G0450, 33F24J0305, 33F24K0211, 33F24L0543, 33F24L0558, 33F25A0540, 33F25C0896, 33F25E0167, 33F25G0119, 33F25H0104, 33F25J0525, 33F25K0412, 33F25L0339, 33F26B0648, 33F26B0666, 33F26C0588
1510801902193275ASK-04510-IHC1/10801902193275/33F24J0306, 33F24L0699, 33F25C0157, 33F25C0782, 33F25E0168, 33F25H0105, 33F25L0475
161080190211804910801902193275ASK-04510-MSK2/10801902118049, 10801902193275/33F24A0872, 33F24B0290, 33F24D0150, 33F24E0461, 33F24G0453, 33F24J0594, 33F25A0541, 33F25C0852, 33F25E0170, 33F25H0740
171080190219327510801902224177ASK-04510-NS/10801902193275, 10801902224177/33F25K0324, 33F26B0653
181080190219327510801902119824FS-04510-S/10801902193275, 10801902119824/33F24L0738, 33F25C0188, 33F25C0755, 33F25L0426, 33F26B0657
191080190211985510801902193275HF-04510-1/10801902119855, 10801902193275/33F24D0036, 33F24G0537, 33F24J0652, 33F24L0576, 33F25A0593, 33F25C0897, 33F25E0260, 33F25E1044, 33F25H0166, 33F25J0936, 33F26B0652, 33F26B0675
2010801902193275ASK-04020-BSM/10801902193275/33F24J0365, 33F24M0075, 33F25A0079, 33F25B0312, 33F25D0116, 33F25D0297, 33F25E0367, 33F25F0400, 33F25G0653, 33F25J0983, 33F25L0155
Amount recalled
310,606

This recall covers 35 products

The agency filed one notice per product. You are reading one of them; the other 34 are below.

22 more are in the archive.

Where it was sold

Why it was recalled

Stop using this product now

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.

Using this product could cause serious injury, illness or death — stop using it now.

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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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:37 PM UTC

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