State

Arkansas product recalls

72,907 recalls have nationwide distribution and so reach Arkansas. 5,513 additional recalls listed Arkansas specifically in their distribution scope.

What the numbers show

Total: 5,513
Critical: 1,018
Severe: 1,210
Most recent: 2026-09-09

Of the 5,513 recalls naming Arkansas we have scored against our rubric, 1,018 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,210 (22%) are Severe.

Which agencies issued them

These figures cover only the 5,513 recalls whose distribution notice names Arkansas specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1201–1225 of 78420

HighFDA (Devices)·Z-2514-2026·2026-06-24
BD Connecta stopcock Port C may over thread rather than tightening
BD Connecta BD Luer-Lok 360 stopcocks, REF 394910, are being recalled because the Port C connection may over thread or spin rather than tightening securely. 2,465,500 units affected.
Product
BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta" Stopcocks are used to administer fluids or medication through one or two different ports via an IV cannula or extension tube. The ports can be used to sample blood or for hemodynamic monitoring.
Category
Medical Device
Distribution
39 states
HighFDA (Devices)·Z-2501-2026·2026-06-24
Medline labour delivery and vaginal kits contain substandard catheters
Medline labour and delivery and vaginal procedure kits are being recalled because representative samples did not meet applicable catheter performance specifications. 24,388 units affected.
Product
MEDLINE Medical Procedure Kits labeled as: 1) BR L&D PACK, Medline Kit Number/SKU DYNJ47625B; 2) GYN VAGINAL, Medline Kit Number/SKU DYNJ912219; 3) KIT MAJ VAG SET UP, Medline Kit Number/SKU DYNJ907033B; 4) MINOR VAG PACK, Medline Kit Number/SKU DYNJ68663B; 5) OB DELIV
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2505-2026·2026-06-24
Medline gynaecology procedure packs contain catheters failing performance specifications
Medline gynaecology procedure packs including hysteroscopy, D&C and tubal ligation kits are being recalled because sample catheters did not meet performance specifications. 37,324 units affected.
Product
MEDLINE Medical Procedure Kits labeled as CLOVIS HYSTEROSCOPY, CSC-N PELVISCOPY, D AND C PACK, D&C HYSTER PACK, FLWR GYN PACK, FS LAP TUBAL LIGATION, HILLSDALE D&C / HYSTEROSCOPY, LAVH NEW BRAUNFELS,TVH PACK, etc (see recall documents for a full list of affected products)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2495-2026·2026-06-24
Medline urethroplasty kits contain catheters failing performance specifications
Medline urology urethroplasty procedure kits are being recalled because representative samples did not meet applicable catheter performance specifications. 91 units are affected.
Product
MEDLINE Medical Procedure Kits labeled as: 1) KIT UROLOGY URETHROPLASTY, Medline Kit Number/SKU DYKMBNDL117C; 2) URETHROPLASTY, Medline Kit Number/SKU DYNJ908978; 3) URETHROPLASTY, Medline Kit Number/SKU DYNJ908978F.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2461-2026·2026-06-24
Stryker Triathlon size 3 baseplate packaging contained a size 4 implant
Triathlon Universal Baseplate Size 3 packaging is being recalled after Stryker identified that it contained a Size 4 baseplate, and vice versa. Seven units are affected.
Product
TRI TS BASEPLATE SIZE 3. Part Number: 5521-B-300.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2488-2026·2026-06-24
Medline cardiovascular and peripheral vascular packs contain substandard catheters
Medline CV and peripheral vascular procedure kits are being recalled because representative samples did not meet applicable catheter performance specifications. 1,248 units affected.
Product
MEDLINE Medical Procedure Kits labeled as: 1) BNT CV PACK, Medline Kit Number/SKU DYNJ912271; 2) CV PACK PART 1, Medline Kit Number/SKU DYNJ31204D; 3) KIT PERIPHERAL VASCULAR MMC, Medline Kit Number/SKU DYNJ905368D; 4) KIT PERIVASCULAR MMC, Medline Kit Number/SKU DYNJ905
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2492-2026·2026-06-24
Medline Robinson 22 Fr catheter packs fail performance specifications
Medline CATH 22F Robinson sterile 5-packs are being recalled because representative samples did not meet applicable catheter performance specifications. 1,000 units are affected.
Product
MEDLINE Medical Procedure Kits labeled as: CATH 22F ROBINSON STRL 5'S PK, Medline Kit Number/SKU DYNJ0040839
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2451-2026·2026-06-24
Medtronic O-arm O2 imaging systems may produce image artifacts
Medtronic O-arm O2 Imaging Systems are being recalled because an anomaly in the detector panel firmware may cause image artifacts. 589 units are affected.
Product
Medtronic O-arm O2 Imaging System. Model Number: BI70002000.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2502-2026·2026-06-24
Medline pelvic laparoscopy packs contain catheters failing performance specifications
Medline Pelvic Lap Packs are being recalled because representative samples did not meet applicable catheter performance specifications. 20 units are affected.
Product
MEDLINE Medical Procedure Kits labeled as: PELVIC LAP PACK, Medline Kit Number/ SKU DYNJ53820B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2471-2026·2026-06-24
ConMed AirSeal 5mm 100mm optical obturator ports may trigger overpressure alerts
ConMed AirSeal 5 mm Access Ports with Low Profile Bladeless Optical Tip Obturators, 100 mm length, are being recalled because of the potential for overpressure alerts.
Product
ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS5-100LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2465-2026·2026-06-24
ConMed AirSeal 12mm access ports may trigger overpressure alerts
ConMed AirSeal 12 mm Access Ports and Obturators with Blunt Tip are being recalled because of the potential for overpressure alerts. 891 packs, or 5,346 units, are affected.
Product
ConMed AirSeal 12 mm Access Port and Obturator with Blunt Tip, 120mm Length. Catalog Number: iASB12-120. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0594-2026·2026-06-24
Aripiprazole 30mg bottle contained voriconazole 50mg tablets instead
Aripiprazole Tablets USP 30 mg from Ajanta Pharma are being recalled after a bottle containing Voriconazole Tablets 50 mg was labelled and distributed as aripiprazole. 6,143 bottles affected.
Product
ARIPIPRAZOLE — ARIPIPRAZOLE (ARIPIPRAZOLE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2508-2026·2026-06-24
Medline CRANI procedure kits contain catheters failing performance specifications
Medline CRANI procedure kits are being recalled because representative samples did not meet applicable catheter performance specifications. 3,521 units are affected.
Product
MEDLINE Medical Procedure Kits labeled as: 1) CRANI, Medline Kit Number/SKU DYNJ908097; 2) CRANI, Medline Kit Number/SKU DYNJ908097A; 3) CRANI, Medline Kit Number/SKU DYNJ908097B; 4) CRANI, Medline Kit Number/SKU DYNJ908097C; 5) CRANI, Medline Kit Number/SKU DYNJ908097
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2482-2026·2026-06-24
Medline red rubber urethral catheterization trays fail performance specifications
Medline Urethral Catheterization Trays with red rubber latex catheter, 15 Fr, are being recalled across all lots because samples did not meet performance specifications. 235,658 units affected.
Product
MEDLINE Urethral Catheterization Tray and Bag, Red Rubber Latex, 15 Fr, Medline Product Number/SKU (REF) DYND18350
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2479-2026·2026-06-24
Medline red rubber urethral catheters fail applicable performance specifications
Medline Urethral Catheters in red rubber latex, spanning French sizes 08 to 22, are being recalled because samples did not meet performance specifications. 2,237,471 units affected.
Product
MEDLINE Urethral Catheter, Red Rubber Latex, Medline Product Number/SKU (REF), French sizes: 1. DYND13508 - 08 Fr; 2. DYND13510 - 10 Fr; 3. DYND13512 - 12 Fr; 4. DYND13514 - 14 Fr; 5. DYND13515 - 15 Fr; 6. DYND13516 - 16 Fr; 7. DYND13518 - 18 Fr; 8. DYND13520 - 20 Fr;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2469-2026·2026-06-24
ConMed AirSeal 5mm 75mm optical obturator ports may trigger overpressure alerts
ConMed AirSeal 5 mm Access Ports with Low Profile Bladeless Optical Tip Obturators, 75 mm length, are being recalled because of the potential for overpressure alerts.
Product
ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 75mm Length. Catalog Number: iAS5-75LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2462-2026·2026-06-24
Stryker Triathlon size 4 baseplate packaging contained a size 3 implant
Triathlon Universal Baseplate Size 4 packaging is being recalled after Stryker identified that it contained a Size 3 baseplate, and vice versa. Seven units are affected.
Product
TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2497-2026·2026-06-24
Medline bioburden test and cystectomy kits contain substandard catheters
Medline procedure kits including the Bioburden Test Kit and Kit Uro Robot Cystectomy are being recalled because sample catheters did not meet performance specifications. 123,030 units affected.
Product
MEDLINE Medical Procedure Kits labeled as BIOBURDEN TEST KIT, Kit Uro Robot Cystectomy, etc. (see the recall documents for a full list of products)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2483-2026·2026-06-24
Medline 14 Fr coude latex catheters fail performance specifications
Medline Intermittent Latex Coude Catheters pre-connected to a collection bag, 14 Fr, are being recalled across all lots because samples did not meet performance specifications. 8,260 units affected.
Product
MEDLINE Intermittent Latex Catheter Coude Pre-Connected to Collection Bag, 14 Fr, 1000mL, Medline Product Number/SKU (REF) URO4RR14C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2490-2026·2026-06-24
Medline oral restoration kits contain catheters failing performance specifications
Medline Oral Restoration procedure kits are being recalled because representative samples did not meet applicable catheter performance specifications.
Product
MEDLINE Medical Procedure Kits labeled as: ORAL RESTORATION, Medline Kit Number/SKUDYNJ86253A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2481-2026·2026-06-24
Medline pre-connected urethral catheterization trays fail performance specifications
Medline Pre-connected Urethral Catheterization Trays with red rubber latex catheter, 15 Fr, are being recalled across all lots. The action covers 4,304,669 units.
Product
MEDLINE Pre-connected Urethral Catheterization Tray and Bag, Red Rubber Latex, 15 Fr, Medline Product Number/SKU (REF) DYND10407
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2474-2026·2026-06-24
ConMed AirSeal 12mm palm grip 100mm ports may trigger overpressure alerts
ConMed AirSeal 12 mm Access Ports with Palm Grip Bladeless Optical Tip Obturators, 100 mm length, are being recalled because of the potential for overpressure alerts.
Product
ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS12-100LPI. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2480-2026·2026-06-24
Medline 15 Fr urethral catheterization trays fail performance specifications
Medline Urethral Catheterization Trays with red rubber latex catheter, 15 Fr, are being recalled because samples did not meet performance specifications. 8,327,756 units are affected.
Product
MEDLINE Urethral Catheterization Tray, Red Rubber Latex, Medline Product Number/SKU (REF), French sizes: 1. DYNC1816, 15 Fr; 2. DYND10350, 15 Fr.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V401000·2026-06-24
Airstream Recalls 2025-2027 Vehicles Due to Rooftop Fan Fire Risk
Airstream is recalling 2025-2027 Interstate and 2026 Classic recreational vehicles because a rooftop ventilation fan component may overheat and cause a fire.
Product
AIRSTREAM — AIRSTREAM INTERSTATE, CLASSIC
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2468-2026·2026-06-24
ConMed AirSeal 8mm 100mm optical obturator ports may trigger overpressure alerts
ConMed AirSeal 8 mm Access Ports with Low Profile Bladeless Optical Tip Obturators, 100 mm length, are being recalled because of the potential for overpressure alerts.
Product
ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS8-100LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.
Category
Medical Device
Distribution
Distributed nationwide