State

Arkansas product recalls

72,992 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 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7101–7125 of 78505

HighFDA (Devices)·Z-1552-2025·2025-04-23
BD Pyxis MedBank Receiving Cabinet Software Medication Dispensing Safety Issue
CareFusion 303 is recalling certain BD Pyxis MedBank Receiving Cabinet Software versions because a "Clear All" function may bypass pharmacist validation, potentially allowing incorrect medication dispensing without authorization.
Product
MEDFLEX, REF: 1119-00; MEDBANK MAIN, REF: 1137-00; MEDFLEX 2.0, REF: 1139-00; MEDBANK TOWER MAIN, REF: 1145-00; MEDBANK MINI MAIN, REF: 1147-00 BD PYXIS MEDBANK Facility Software, REF: 139090-01; BD PYXS MEDBNK TWR MN 2HH1FH2HM2FM2FG1FF, REF: 169-100; BD PYXIS MEDBANK MINI 1HH-1F
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1612-2025·2025-04-23
Medline Convenience Kits Recalled for Potential Open Breather Pouch Seals
Medline Industries is recalling select sterile convenience kits (Model DYNJ80807B, Lot 24IBH993) due to potential open or weak seals on breather pouches used for packaging. Compromised seals may affect product sterility.
Product
Medline Convenience kits used for various procedures: 1) CW PERI GYN, Model Number: DYNJ80807B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1561-2025·2025-04-23
TLX/TLC SP Guided Implant Driver missing laser marked depth markings
Straumann USA LLC is recalling TLX/TLC SP Guided Implant Driver units because they are missing laser marked depth markings, which may affect proper surgical placement.
Product
TLX/TLC SP Guided Implant Driver, for ratchet, stainless steel; REF: 037.3002;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1553-2025·2025-04-23
Philips DXR System X-Ray Equipment Collimator Fall Hazard Recall
Philips is recalling certain DXR System DuraDiagnost 4.1 stationary X-ray systems due to a potential for the collimator to fall if installed incorrectly.
Product
Philips DXR System, DuraDiagnost 4.1. Stationary X-Ray System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1617-2025·2025-04-23
Medline Sterile Ophthalmic Convenience Kits Recalled for Weak Breather Pouches
Medline Industries is recalling select sterile ophthalmic convenience kits due to potential open or weak seals on breather pouches used for packaging. The kits are used for various eye procedures.
Product
Medline Convenience kits used for various procedures: 1) BASIC CATARACT, Model Number: DYNJ41097A; 2) PK EYE, Model Number: DYNJ60631B; 3) CATARACT PACK, Model Number: DYNJ80316A; 4) BASIC EYE PACK, Model Number: DYNJ63707C; 5) EYE PACK WITH ACCESSORY PACK, Model Number:
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1588-2025·2025-04-23
Medline sterile convenience kits recalled for weak breather pouch seals
Medline is recalling two models of sterile convenience kits (PAIN PACK and PAIN TRIAL PACK) due to potential open or weak seals on breather pouches used in the packaging.
Product
Medline Convenience kits used for various procedures: 1) PAIN PACK, Model Number: DYNJ67577A; 2) PAIN TRIAL PACK, Model Number: DYNJ67576A;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1556-2025·2025-04-23
GE Venue Fit ultrasound systems battery fire hazard recall
GE Medical Systems is recalling certain Venue Fit ultrasound systems because the battery can develop an internal failure that could result in smoke or fire.
Product
Venue Fit Models: R3 (Model Number H45303VFSC, H45303VFSW), R4 (Model Number H45314VFS, H45314VFSW), Venue Fit R5 system (Model Numbers H45335VFS, H45335VFSW), R3 Surgery for China, R3 PeriOP for China, R3 Expert for China, R3 Pro for China, R3 Performance for China, R3 Intervent
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1591-2025·2025-04-23
Medline Sterile Convenience Kits Recalled for Weak Breather Pouch Seals
Medline Industries is recalling sterile convenience kits for various medical procedures due to potential open or weak seals on breather pouches used in product packaging.
Product
Medline Convenience kits used for various procedures: 1) ANGIOGRAPHY DRAPE PACK, Model Number: HCP075G; 2) ENSEMBLE CORONAROGRAPHIE-LF, Model Number: DYNJ64354A; 3) RADIOL ANGIO PACK-LF, Model Number: 0M-CP01029D; 4) ARTERIOGRAM PACK 2, Model Number: DYNJ81454B; 5) CATH
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1589-2025·2025-04-23
Medline Convenience Kits Recalled for Potential Open or Weak Seals
Medline Industries is recalling select sterile convenience kits due to potential open or weak seals on breather pouches used for packaging. The defect may compromise product sterility.
Product
Medline Convenience kits used for various procedures: 1) CUSTOM BLOCK KEMP PACK-LF, Model Number: DYNJ0371999G;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1609-2025·2025-04-23
Medline Hernia Repair Convenience Kit Recalls Due to Weak Seals
Medline is recalling Hernia Repair Tote convenience kits (Model DYNJ908337C) because purchased breather pouches used for packaging may have open or weak seals, which could compromise product sterility.
Product
Medline Convenience kits used for various procedures: 1) HERNIA REPAIR TOTE, Model Number: DYNJ908337C
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1606-2025·2025-04-23
Medline Convenience Kit Skin Lesion Set Potential Seal Defect
Medline is recalling its Skin Lesion Set convenience kits due to potential open or weak seals on breather pouches used for packaging. The compromised seals may affect the sterility of the kits.
Product
Medline Convenience kits used for various procedures: 1) SKIN LESION SET, Model Number: MNS6270
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1613-2025·2025-04-23
Medline Convenience Kits Recalled for Potentially Open Breather Pouches
Medline Industries is recalling 706 units of various sterile convenience kits used for gynecological and other procedures due to potential open or weak seals on breather pouches. The packaging defect could affect product sterility.
Product
Medline Convenience kits used for various procedures: 1) STANDARD D&C, Model Number: DYNJ69733; 2) NHS - LAP BOWEL GNG, Model Number: DYNJ39904A; 3) LAPAROSCOPY GYN SURGERY PA, Model Number: DYNJ64651A; 4) GYNE - LITHOTOMY MAJOR-LF, Model Number: DYNJ49250F; 5) ENS. GYNE
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1577-2025·2025-04-23
Maquet VH-3010 Power Supply Recalled for Inadequate Heating Function
Maquet Cardiovascular is recalling 110 units of the VH-3010 Power Supply due to an incorrect resistor that may prevent the HemoPro 2 harvesting tool jaws from heating adequately.
Product
Maquet VH-3010 Power Supply. Used to deliver power to the harvesting tool of the Vasoview Hemopro EVH System (HemoPro 2).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1573-2025·2025-04-23
ID NOW RSV 24T Respiratory Virus Assay System Higher Invalid Result Rates
Abbott Diagnostics is recalling certain lots of the ID NOW RSV 24T respiratory virus assay system due to higher-than-expected invalid result rates compared to the product instructions.
Product
Brand Name: ID NOW RSV 24T Product Name: ID NOW RSV 24T Model/Catalog Number: 435-000 Software Version: N/A Product Description: Respiratory virus panel nucleic acid assay system Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1601-2025·2025-04-23
Medline Convenience Kits Recalled for Potential Weak Breather Pouch Seals
Medline Industries is recalling select sterile convenience kits due to potential open or weak seals on breather pouches used for packaging. The issue affects 116 units distributed worldwide.
Product
Medline Convenience kits used for various procedures: 1) MINOR BASIN -SMH, Model Number: DYNJ907733B
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1605-2025·2025-04-23
Medline Convenience Kit NAIL PACK Sterile Packaging Seal Defect Recall
Medline is recalling select NAIL PACK sterile convenience kits (Model SUT15830A, Lot 24IBR642) due to potential open or weak seals on breather pouches used for product packaging.
Product
Medline Convenience kits used for various procedures: 1) NAIL PACK, Model Number: SUT15830A;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0366-2025·2025-04-23
Chlorpromazine Hydrochloride Tablets Recalled Due to Impurity
The FDA is recalling Chlorpromazine Hydrochloride Tablets, 10 mg, due to the presence of N-Nitroso-Desmethyl Chlorpromazine impurity above recommended limits. The affected lot was distributed nationwide.
Product
ChlorproMAZINE Hydrochloride Tablets, USP, 10 mg, packaged in cartons of 100 TABLETS (10x10), Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268, NDC 0904-7129-61
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1587-2025·2025-04-23
Medline Convenience Kits Rhinoplasty Pack Potential Weak Seals Recall
Medline Industries is recalling Rhinoplasty Pack convenience kits (Model DYNJ84116A, Lot 24IBH580) due to potential open or weak seals on breather pouches used for packaging. Compromised packaging may affect sterility of the sterile kits.
Product
Medline Convenience kits used for various procedures: 1) RHINOPLASTY PACK, Model Number: DYNJ84116A
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1571-2025·2025-04-23
ID NOW COVID-19 2.0 Point-of-Care Test Device Recall
Abbott is recalling certain lots of the ID NOW COVID-19 2.0 24T test device due to higher invalid result rates than stated in product instructions. The affected lots were distributed worldwide.
Product
Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID NOW COVID-19 2.0 24T Model/Catalog Number: 192-000 Software Version: N/A Product Description: Simple Point-Of-Care Device To Detect Sar-Cov-2 Nucleic Acid Targets Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1602-2025·2025-04-23
Sterile convenience kits recalled for potentially weak breather pouch seals
Medline Industries is recalling sterile convenience kits due to potential open or weak seals on breather pouches used in packaging. Defective seals may compromise product sterility.
Product
Refer to RES
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1578-2025·2025-04-23
Rover Mobile X-ray System Recalled for Potential Early Tube Failure
Micro-X Ltd. is recalling 31 Rover Mobile X-ray Systems (Model MXU-RV71) due to potential early life failure of the x-ray tube caused by excessive thermal load on the anode. The systems were distributed nationwide in California, New Jersey, and Puerto Rico.
Product
Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number: MXU-RV71 Product Description: Rover Mobile X-rays System ("Rover") is a mobile imaging system that incorporates a self-contained X-ray generator, imaging display and software for acquiring medical diagn
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1576-2025·2025-04-23
ID NOW RSV 24T Respiratory Virus Panel Has Higher Invalid Test Rates
Abbott Diagnostics is recalling specific lots of the ID NOW RSV 24T respiratory virus assay due to higher-than-expected invalid test rates. The affected lots were distributed nationwide.
Product
Brand Name: ID NOW RSV 24T Product Name: ID NOW RSV 24T Model/Catalog Number: 435-000 Software Version: N/A Product Description: Respiratory virus panel nucleic acid assay system Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0714-2025·2025-04-23
Tony's Chocolonely Dark Chocolate Almond Sea Salt recalled for foreign objects
Tony's Chocolonely Dark Chocolate Almond Sea Salt is being recalled nationwide because some units contain stones. Consumers who have purchased affected lots should not consume the product.
Product
Tony's Chocolonely Dark Chocolate Almond Sea Salt
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1597-2025·2025-04-23
Medline Convenience Kits Recalled for Potentially Open Breather Pouches
Medline Industries is recalling select sterile convenience kits because purchased breather pouches used for packaging may have open or weak seals, potentially compromising the sterility of the kits.
Product
Medline Convenience kits used for various procedures: 1) T A PACK, Model Number: DYNJ67791A; 2) NASAL PACK, Model Number: DYNJ66514; 3) ENT PACK, Model Number: DYNJ67775A; 4) T/A ENDO PACK, Model Number: DYNJ83158; 5) T & A PACK, Model Number: DYNJ0634878I; 6) PPM-IC
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1619-2025·2025-04-23
Medline Sterile Convenience Kits Recalled for Open Breather Pouches
Medline Industries is recalling three models of sterile convenience kits used for arthroscopy procedures due to potential open or weak seals on the breather pouches used for packaging.
Product
Medline Convenience kits used for various procedures: 1) ARTHROSCOPIE DU GENOU-LF, Model Number: DYNJ40229A; 2) ARTHROSCOPY PACK-LF, Model Number: OPK382N; 3) ARTHROSCOPY NEW TEGH-LF, Model Number: DYNJ46723B
Category
Medical Device
Distribution
Distributed nationwide