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.

1051–1075 of 78420

SevereFDA (Devices)·Z-2602-2026·2026-07-01
Abiomed Impella CP Set with SmartAssist 10th Generation Introducer Kit Recall
Abiomed is recalling Impella CP Set with SmartAssist (10th Generation) containing 14Fr Low Profile Introducer Kits due to potential thrombus (blood clot) formation during prolonged use of the introducer.
Product
Abiomed Impella CP Set with SmartAssist (10th Generation) containing affected 14Fr Low Profile Introducer Kits 13 and 25 cm Japan. Product Code: 1000542.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2591-2026·2026-07-01
Medline angiography and radiology convenience kits recalled for unapproved design changes
Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA clearance. The recall affects 113,843 kits distributed nationwide and to Barbados.
Product
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ANGIO PACK DYNJ30565C DYNJ32555B ANGIO PACK-LF DYNJ0774765U ANGIO TRAY DYNJ46153A ANGIOGRAM TRAY DYNJ33638K ANGIOGRAPHY DRAPE PK QVH-LF DYNJ35110D ANGIOGRAPHY P
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0623-2026·2026-07-01
ChloraPrep One-Step Topical Solution Sterility Assurance Recall
CareFusion 213, LLC is recalling ChloraPrep One-Step (chlorhexidine gluconate and isopropyl alcohol) due to wrinkles in the paper lidding that may breach the seal, compromising sterility assurance.
Product
CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-1123-2026·2026-07-01
Sunflower Seeds Recalled for Undeclared Cashew Allergen
George J Howe Company, Inc. is recalling 25-pound cases of sunflower seeds due to the presence of undeclared cashew, a tree nut allergen. The product was distributed across multiple states.
Product
25# Sunflower Seeds C/S
Category
Food
Distribution
25 states
SevereFDA (Devices)·Z-2592-2026·2026-07-01
Medline Polycarbonate Syringes in Convenience Kits Recalled for Unapproved Design Changes
Medline Industries recalled multiple convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA clearance. The company identified these modifications and notified the FDA of the deviation from the approved 510(k) design.
Product
Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ANGIO DRAPE PACK (ADLUG)642-LF DYNJ47665D ANGIO PACK DYNJ30565D ANGIOGRAPHY PACK-LF DYNJ0854485V ARTERIOGRAM DYNJ28082D DYNJ28082F CARDIAC CATH DYNJ67349 CARDIA
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-1117-2026·2026-07-01
Utz Quality Foods Dirty Sour Cream Onion Potato Chips Salmonella Recall
Utz Quality Foods is recalling 2.0 oz bags of Dirty Sour Cream and Onion Potato Chips due to potential Salmonella contamination. The product was distributed across 32 US states.
Product
2.0 oz Dirty Sour Cream and Onion Potato Chips, Plastic Bag.
Category
Food
Distribution
34 states
SevereFDA (Food)·H-1116-2026·2026-07-01
Zapp's Big Cheezy Potato Chips recalled due to Salmonella risk
Utz Quality Foods, LLC is recalling 1.5oz and 8.0oz bags of Zapp's Big Cheezy Potato Chips due to potential Salmonella contamination. The recalled product was distributed across 32 states.
Product
1.5oz, 8.0oz , Zapp's Big Cheezy Potato Chips, Plastic Bag.
Category
Food
Distribution
34 states
SevereFDA (Devices)·Z-2455-2026·2026-07-01
Medline Convenience Kits Medical Devices Recalled for Quality Issues
Medline Industries is recalling four models of Convenience Kits containing Lidocaine and Bupivacaine injections due to quality issues identified during an FDA inspection of the supplier.
Product
Medline Convenience Kits: 1) DRAWER 6A ADULT CENTRAL LINE, Model Number: ACC010890; 2) OPEN HEART A OVERHEAD, Model Number: DYNJ910066; 3) OPEN HEART, Model Number: DYNJ9855016V; 4) OPEN HEART, Model Number: DYNJ9855016X
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-1114-2026·2026-07-01
Dirty Brand Salt and Vinegar Potato Chips Recalled for Salmonella
Utz Quality Foods is recalling 1.5 oz and 2 oz bags of Dirty Brand Salt and Vinegar Potato Chips due to potential Salmonella contamination. The affected products were distributed across 32 states.
Product
1.5oz, 2oz Dirty Brand Salt and Vinegar Potato Chips , Plastic Bag.
Category
Food
Distribution
34 states
SevereFDA (Devices)·Z-2453-2026·2026-07-01
Medline Convenience Kits with Lidocaine and Bupivacaine Injections Recalled
Medline Industries is recalling 22 models of Convenience Kits that contain Lidocaine Hydrochloride Injection and Bupivacaine Hydrochloride in Dextrose Injection due to quality issues found during an FDA inspection of the supplier.
Product
Medline Convenience Kits: 1) OPEN HEART CDS, Model Number: CDS840144Q; 2) OPEN HEART, Model Number: CDS840150W; 3) OPEN HEART ADULT, Model Number: CDS840396AA; 4) CABG A CDS, Model Number: CDS982269N; 5) OPEN HEART ANESTHESIA PACK, Model Number: CDS983849G; 6) OPEN HE
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2452-2026·2026-07-01
Medline Convenience Kits containing anesthesia components recalled for quality issues
Medline Industries is recalling Medline Convenience Kits (models DYNJ905503F and DYNJ905503G) that contain Arrow Kits with Lidocaine Hydrochloride Injection and Bupivacaine Hydrochloride in Dextrose Injection due to quality issues found during an FDA inspection of the supplier.
Product
Medline Convenience Kits: 1) DYNJ905503F, Model Number: CV ANESTHESIA - ROOM SET UP; 2) DYNJ905503G, Model Number: CV ANESTHESIA - ROOM SET UP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-1112-2026·2026-07-01
Zapp's Bayou Blackened Ranch Kettle Chips Recalled for Salmonella
Utz Quality Foods, LLC is recalling 1.5oz bags of Zapp's Bayou Blackened Ranch Kettle Chips due to the potential presence of Salmonella. The product was distributed across 32 states.
Product
1.5oz Zapp's Bayou Blackened Ranch Kettle Chips, Plastic Bag.
Category
Food
Distribution
34 states
SevereFDA (Devices)·Z-2600-2026·2026-07-01
Abiomed Impella CP Introducer Kit Recalled for Thrombus Risk
Abiomed is recalling the 14 Fr x 25 cm Low Profile Introducer Kit for Impella CP due to potential thrombus formation during prolonged use. The recall affects 17 units distributed in the United States and Japan.
Product
Abiomed 14 Fr x 25 cm Low Profile Introducer Kit for Impella CP. Impella Set Product Code: 1000435. Introducer Product Code: 1000435.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2521-2026·2026-07-01
Da Vinci surgical system operative components with E-brake retainer pin defect
Intuitive Surgical recalls certain Da Vinci surgical system operative components due to a defective E-brake retainer pin that may fail to engage the E-brake, potentially causing uncontrolled motion and patient injury.
Product
Da Vinci ASSY, PSS, SP1098, Part Number: 380601
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-1100-2026·2026-07-01
Spring & Mulberry Mango Chili Date-Sweetened Chocolate bars recalled
Spring & Mulberry Inc. is recalling Spring & Mulberry Mango Chili Date-Sweetened Chocolate bars nationwide due to potential Salmonella contamination. Consumers should not consume the product and should dispose of it or return it.
Product
Spring & Mulberry Mango Chili Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in an orange box, UPC 850055470033, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold indi
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2560-2026·2026-07-01
Surgify Halo surgical burr recalled for potential breakage risk
Surgify Medical is recalling the Surgify Halo 4.0 mm surgical burr because it may break during bi-portal endoscopic spinal surgery. The device is distributed nationwide.
Product
Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.070.NVG.H1; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2531-2026·2026-07-01
Zimmer Off-Axis Alliance Glenoid Reamer Guide recalled for breakage
Zimmer is recalling the Off-Axis Alliance Glenoid Right 4-Peg Augment Reamer Guide (Model 110040476) after five complaints that plastic guides broke during reaming.
Product
Off-Axis Alliance Glenoid, Right, 4-Peg, Augment, Reamer Guide, Model/Catalog Number: 110040476
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2569-2026·2026-07-01
Surgify Halo Surgical Burrs Subject to Potential Breakage Recall
Surgify Halo 5.4 mm surgical burrs may break during bi-portal endoscopic spinal surgery. The FDA has classified this as a Class II recall affecting devices distributed nationwide.
Product
Surgify Halo, 5.4 mm, Medium, Model/Catalog Number: 54.085.SHD.U1; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2557-2026·2026-07-01
Surgify Halo surgical drill recalled for potential burr breakage
Surgify Halo 3.0 mm surgical drills may experience burr breakage during bi-portal endoscopic spinal surgery. The FDA is requesting the recall of this device across multiple US states.
Product
Surgify Halo, 3.0 mm, Long, Model/Catalog Number: 30.125.NVG.U2; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26E040000·2026-07-01
Chrysler Recalls MOPAR Headlights Due to Lighting Failure Risk
Chrysler is recalling specific MOPAR headlight assemblies because wiring defects may cause lights to flicker or fail, reducing vehicle visibility.
Product
EXTERIOR LIGHTING:HEADLIGHTS recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2556-2026·2026-07-01
Surgify Halo surgical drill equipment recalled for potential burr breakage
Surgify Halo 3.0 mm Short surgical drills and burrs are being recalled because they may break during bi-portal endoscopic spinal surgery, potentially leaving fragments in the patient.
Product
Surgify Halo, 3.0 mm, Short, Model/Catalog Number: 30.070.NVG.U2; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2571-2026·2026-07-01
Surgify Halo surgical burrs recalled for potential breakage during spinal surgery
Surgify Medical OY is recalling Surgify Halo 5.4 mm Long surgical burrs due to potential breakage during bi-portal endoscopic spinal surgery. The defect could affect patient safety during the procedure.
Product
Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.125.NVG.U1; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2565-2026·2026-07-01
Surgify Halo Surgical Burr Recalling Potential Tool Breakage Risk
SURGIFY MEDICAL OY is recalling the Surgify Halo 5.4 mm Extendable surgical burr due to risk of burr breakage during bi-portal endoscopic spinal surgery (BESS). The recalled units are distributed nationwide.
Product
Surgify Halo, 5.4 mm, Extendable, Model/Catalog Number: 54.000.SEE.U1; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2580-2026·2026-07-01
Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump recall
Boston Scientific Corporation is recalling the Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump (model AP-0300H) due to potential leakage along the drug pathway from the pump through the catheter.
Product
Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2570-2026·2026-07-01
Surgify Halo surgical burrs recalled for potential breakage risk
Surgify Medical is recalling the Surgify Halo 5.4 mm surgical burrs due to potential breakage during spinal surgery procedures.
Product
Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.125.NVG.H1; drills, burrs, trephines & accessories (simple, powered)
Category
Medical Device
Distribution
Distributed nationwide