Arrow International, LLC recalls
47 recalls filed under Arrow International, LLC. The most recent was published June 24, 2026.
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Class I · 4 months ago
Arrow International, LLC Description/REF: RA CATH KIT: 20 GA X 1-3/4IN/AK-04020-SPC recall: Lidocaine, Bupivacaine, and 0.9% sodium chloride
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…
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Class I · 4 months ago
Arrow International, LLC Description/REF: Access Tray/ASK-04001-MC3 recall: Lidocaine, Bupivacaine, and 0.9% sodium chloride
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…
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Class I · 4 months ago
Arrow International, LLC Description/REF: Access Tray/ASK-04001-JHH recall: Lidocaine, Bupivacaine, and 0.9% sodium chloride
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…
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Class I · 4 months ago
Arrow International, LLC Description/REF: PI Midline 2L: 5FR X 20CM/CDC-32052-Mpkc recall: Lidocaine, Bupivacaine, and 0.9% sodium chloride
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…
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Class I · 4 months ago
Arrow International, LLC Description/REF: PI Agba Picc KIT: 3L 6 FR X 40 CM recall: Lidocaine, Bupivacaine, and 0.9% sodium chloride
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…
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Class I · 4 months ago
Arrow International, LLC Description/REF: Arterial Line KIT: SL 20 GA X 5 recall: Lidocaine, Bupivacaine, and 0.9% sodium chloride
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…
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Class I · 4 months ago
Arrow International, LLC Description/REF: Paracentesis KIT/ASK-00376-JHH recall: Lidocaine, Bupivacaine, and 0.9% sodium chloride
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…
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Class I · 4 months ago
Arrow International, LLC Description/REF: Access Tray/GU-04020 recall: Lidocaine, Bupivacaine, and 0.9% sodium chloride
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…
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Class I · 4 months ago
Arrow International, LLC Description/REF: Hemodialysis KIT: 2-Lumen 12 FR X 20 recall: Lidocaine, Bupivacaine, and 0.9% sodium chloride
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…
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Class I · 4 months ago
Arrow International, LLC Description/REF: Epidural Catheter KIT: 19 GA X 90 recall: Lidocaine, Bupivacaine, and 0.9% sodium chloride
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…
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Class I · 4 months ago
Arrow International, LLC Description/REF: PI Jacc KIT: 2L 5.5 FR X 15 CM recall: Lidocaine, Bupivacaine, and 0.9% sodium chloride
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…
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Class I · 5 months ago
Arrow International, LLC Cannon II Plus Hemodialysis Catheter, REF: CS-15242-VSP recall: 16F dual-valved splittable sheath introducer
16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer…
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Class I · 5 months ago
Arrow International, LLC NextStep Antegrade Chronic Hemodialysis Catheter recall: 16F dual-valved splittable sheath introducer
16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer…
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Class I · 5 months ago
Arrow Edge Hemodialysis Catheterization Product recall: 16F dual-valved splittable sheath introducer
16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer…
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Class I · 5 months ago
Arrow-Clark VectorFlow Antegrade Chronic Hemodialysis Catheter: REF recall: 16F dual-valved splittable sheath introducer
16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer…
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Class II · 6 months ago
Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use recall: Due to receiving a notice from a supplier that the liquid adhesive
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
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Class II · 6 months ago
Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code recall: Due to receiving a notice from a supplier that the liquid adhesive
Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured
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Class II · 6 months ago
Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC Kit REF recall: Due to receiving a notice from a supplier that the liquid adhesive
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
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Class II · 6 months ago
Arrow International, LLC Percutaneous Sheath Introducer with 7.5 - 8 Fr. Catheter REF recall: Due to receiving a notice from a supplier that the liquid adhesive
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
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Class II · 6 months ago
Arrow International, LLC Flextip Plus Epidural Catheter recall: Due to receiving a notice from a supplier that the liquid adhesive
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
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Class II · 6 months ago
Arrow, Arrowg+ARD AND Arrowg+ARD Blue Plus Pressure Injectable Central recall: Due to receiving a notice from a supplier that the liquid adhesive
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
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Class II · 6 months ago
Arrow Radial Artery Catheterization KIT REF ASK-04220-UCL1 UDI code recall: Due to receiving a notice from a supplier that the liquid adhesive
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
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Class II · 6 months ago
Arrow International, LLC MAC" Two-Lumen Central Venous Access Kit for use with 7.5 recall: Due to receiving a notice from a supplier that the liquid adhesive
Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
About this page
Arrow International, LLC appears here because a federal agency named it as the recalling firm or the brand on the label. A recall is not a judgement about everything the company sells — it covers only the lot codes and models listed in each notice.