Every recall we track for ARROW INTERNATIONAL, LLC — 47 in all — plus the complaints and injury reports the public filed about them.
Arrow recalls specific PICC G4 stylet kits due to potential contamination with lidocaine, bupivacaine, and saline. If sterility is compromised, serious or life-threatening injuries may occur. Affected units include certain model numbers and batch codes.
Arrow recalls multiple hemodialysis kits due to potential sterility issues with lidocaine, bupivacaine, and saline solutions, which could cause serious or life-threatening injuries if not properly sterilized.
Arrow recalls specific CVC kits due to potential contamination of lidocaine, bupivacaine, and saline. If the product is not sterile, it could cause serious or life-threatening injuries.
Arrow recalls certain PICC kits due to potential sterility issues in injectable products, which could lead to serious or life-threatening injuries. Affected kits include specific models and batch numbers.
Arrow recalls specific Pacing PSI kits due to potential sterility issues with lidocaine, bupivacaine, and saline solutions, which could cause serious or life-threatening injuries if not properly sterilized.
Arrow recalls paracentesis kits with potential contamination of lidocaine, bupivacaine, and saline. If sterility is compromised, serious or life-threatening injuries may occur. Affected kits have specific reference numbers.
Arrow recalls specific drainage and thoracentesis kits due to potential contamination of lidocaine, bupivacaine, and saline solutions, which could cause serious or life-threatening injuries if sterility is compromised.
Arrow International LLC recalls antimicrobial PSI medical kits due to potential sterility issues that could lead to serious or life-threatening injuries. Check product model numbers and batch codes for affected items.
Arrow International LLC recalls specific catheter kits due to supplier quality issues with lidocaine, bupivacaine, and saline solutions potentially causing serious or life-threatening injuries if sterility is compromised.
Arrow International recalls specific CVC kits containing lidocaine, bupivacaine, and saline due to potential sterility problems that could cause serious injuries.
Arrow International LLC recalls specific PSI kits due to potential sterility issues in water-based injectables, which could cause serious or life-threatening injuries. Affected kits have model numbers starting with ASK or CDC prefixes.
Arrow recalls biopsy system kits with potential contamination in lidocaine, bupivacaine, or saline solutions that could cause serious injury or illness.
Arrow recalls several medical kits due to potential contamination of sterile products, which could lead to serious or life-threatening injuries if sterility is compromised.
ARROW recalls multiple arterial catheter kits due to potential contamination in lidocaine, bupivacaine, and saline solutions, which could cause serious or life-threatening injuries if sterility is compromised.
Arrow recalls certain Pacing PSI kits due to potential contamination in lidocaine, bupivacaine, and saline solutions. If sterility is compromised, serious or life-threatening injuries may occur. Affected kits have specific batch numbers.
Arrow International LLC recalls specific catheter kits due to potential sterility issues in water-based injectable products, which could lead to serious or life-threatening injuries. Affected kits include various models with specific part numbers.
Arrow recalls peritoneal lavage catheter kits with lot numbers AK-09000/30801902121722 and others due to potential sterility issues that could cause serious infections.
Arrow recalls specific hemodialysis kits due to potential contamination of lidocaine, bupivacaine, and saline. If sterility is compromised, serious or life-threatening injuries may occur. Affected kits have unique batch codes.
Arrow International LLC recalls multiple midline catheter kits and sets due to potential contamination with lidocaine, bupivacaine, and 0.9% sodium chloride. The supplier had quality issues that could lead to serious or life-threatening injuries if sterility is compromised.
Arrow recalls HemoDialysis Kits with CDC-25142-X1A lot numbers due to potential contamination. If sterility is compromised, serious or life-threatening injuries may occur. Affected kits include specific batch numbers.
Arrow recalls specific 18G medical kits (SAC-01218-B/C) for potential sterility problems that could cause serious infections or injuries.
Arrow recalls PICC access trays with specific lot numbers due to potential contamination of lidocaine and bupivacaine. This could lead to serious or life-threatening injuries if the medication is not sterile.
Arrow recalls spinal anesthesia kits with potential sterility issues that could cause serious or life-threatening injuries. Affected kits include specific models and batch numbers. Consumers should contact Arrow for details.
Arrow recalls certain medical kits due to potential sterility issues in injectable products, which could lead to serious or life-threatening injuries if used.
Arrow recalls multiple arterial catheter and vein access kits due to potential contamination in lidocaine, bupivacaine, and saline solutions. Affected kits may cause serious injury if sterility is compromised.
Arrow recalls Access Tray model ASK-04001-MC3 due to potential contamination of lidocaine and bupivacaine in medication kits, which could cause serious or life-threatening injuries if sterility is compromised.
ARROW INTERNATIONAL, LLC
Arrow recalls PI Midline 2L catheters (CDC-32052-MPKC) due to potential contamination in medication kits, which could cause serious or life-threatening injuries if sterility is compromised.
Arrow recalls specific PICC kits due to potential contamination of lidocaine, bupivacaine, and saline solutions which could cause serious or life-threatening injuries if sterility is compromised.
Arrow recalls arterial line kits that may contain contaminated medication, risking serious injury or death. Affected kits include specific models and batch numbers. Consumers should stop using and contact Arrow for details.
Arrow recalls PARACENTESIS KIT (ASK-0:00376-JHH) due to potential contamination in lidocaine, bupivacaine, and saline solutions, which could cause serious or life-threatening injuries if sterility is compromised.
Arrow International LLC recalls medical kits with lidocaine, bupivacaine, and saline due to potential sterility issues. If contaminated, these products could cause serious or life-threatening injuries. Consumers should check product codes and contact Arrow for details.
Arrow International LLC recalls hemodialysis kits that may contain contaminated solutions. If sterility is compromised, serious or life-threatening injuries could occur. Check product codes and batch numbers listed in the recall notice.
Arrow International LLC recalls specific epidural catheter kits due to potential sterility issues in the lidocaine and bupivacaine solutions, which could lead to serious or life-threatening injuries if the product is not sterile.
Arrow recalls specific medical kits due to potential contamination in lidocaine, bupivacaine, and saline solutions. If sterility is compromised, serious or life-threatening injuries may occur. Affected kits include 1L, 2L, and 3L sizes with specific model numbers.
Arrow recalls Cannon II Plus hemodialysis catheters with specific model numbers due to potential sheath splitting issues causing pain, bleeding, and vessel injury during dialysis procedures.
Arrow recalls specific NextStep hemodialysis catheters due to a sheath introducer that may not split properly, leading to pain, bleeding, or tissue injury during dialysis procedures.
Arrow recalls hemodialysis catheter kits with potential for improper splitting, causing pain, bleeding, or vessel injury. Affected kits include specific model numbers and lot codes.
Arrow recalls VectorFlow hemodialysis catheters with potential sheath splitting issues causing pain, bleeding, and vessel injury. Affected models include ACS-15192-VFI and similar codes. Contact Arrow for details.
Arrow recalls two-lumen central venous access kits with incorrect adhesive manufacturing. The product may not function properly due to a supplier error.
Arrow recalls echogenic introducer needles with specific UDI code due to incorrect adhesive manufacturing. Affected units may have safety risks; contact Arrow for details.
Arrow recalls specific Pressure Injectable Arrowg+ard Blue Plus Four-Lumen CVC Kits due to incorrect adhesive manufacturing. This may affect catheter infection prevention safety.
Arrow recalls percutaneous sheath introducers with 7.5-8 Fr catheters (REF ASK-09903-MGH3) due to incorrect liquid adhesive manufacturing. Affected units may have safety risks.
Arrow recalls FLEXTIP Plus Epidural Catheter kits with incorrect adhesive due to supplier error. Affected units have specific UDI codes and batch numbers. Consumers should contact Arrow for details.
Arrow recalls pressure injectable central venous catheters with incorrect adhesive manufacturing. Affected models include ArrowG+ard and ArrowG+ard Blue Plus with specific UDI codes. No immediate action needed but check for the listed batch numbers.
Arrow recalls radial artery catheterization kits with incorrect adhesive manufacturing. Affected kits have specific UDI codes and batch numbers. Consumers should contact Arrow for details.
Arrow recalls MAC Two-Lumen Central Venous Access Kits with incorrect adhesive manufacturing. Affected units have specific UDI codes and batch numbers. Consumers should contact Arrow for details.
