The Recall Desk

State

Arkansas product recalls

73,597 recalls have nationwide distribution and so reach Arkansas. 5,543 additional recalls listed Arkansas specifically in their distribution scope.

What the numbers show

Total
5,543
Critical
1,027
Severe
1,448
Most recent
2026-10-14

Of the 5,543 recalls naming Arkansas we have scored against our rubric, 1,027 (19%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,448 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,543 recalls whose distribution notice names Arkansas specifically. The 73,597 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28551–28575 of 79140

  • HighFDA (Devices)·Z-0374-2021·2020-11-11

    Zimmer Biomet Recalls Acetabular Hip Prosthesis Cups Due to Sterilant Concerns

    Zimmer Biomet is recalling 412 acetabular hip prosthesis cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.

    Product
    ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, 10 degree inclined face, O.D. Cup with Spacers, 53 mm Number: 00-8065-650-32
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0313-2021·2020-11-11

    GE Datex-Ohmeda Aisys CS2 Anesthesia System Recalled for Damaged Flow Sensors

    GE Healthcare is recalling 101 Aisys CS2 Anesthesia Systems because flow sensors may have damaged tubes, posing a risk to patients.

    Product
    GE Datex-Ohmeda Aisys CS2 Anesthesia System - Product Usage: is intended to provide general inhalation anesthesia and ventilatory support to a wide range of patients (neonatal, pediatric adult). The device is intended for volume or pressure control ventilation.
    Category
    Medical Device
    Distribution
    36 states
  • HighFDA (Devices)·Z-0327-2021·2020-11-11

    Zimmer Biomet Recalls Acetabular Hip Prosthesis Cups Due to Sterilant Concerns

    Zimmer Biomet is recalling 412 acetabular hip prosthesis cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.

    Product
    ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, Neutral, O.D. Cup with Spacers, 47 mm Item Number: 00-8065-544-26
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0350-2021·2020-11-11

    Zimmer Biomet Recalls Acetabular Hip Cups Due to Sterilant Biocompatibility Concerns

    Zimmer Biomet is recalling 412 acetabular hip cups because the sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.

    Product
    ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, Neutral, O.D. Cup with Spacers, 59 mm Number: 00-8065-556-26
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0362-2021·2020-11-11

    Zimmer Biomet Recalls Hip Prosthesis Cups Due to Sterilant Biocompatibility Concerns

    Zimmer Biomet is recalling 412 units of ZCA All Poly Acetabular Cups because the sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.

    Product
    ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 28 mm, 10 degree inclined face, O.D. Cup with Spacers, 47 mm Number: 00-8065-644-28
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0386-2021·2020-11-11

    Zimmer Biomet Recalls Hip Prosthesis Components Due to Sterilant Biocompatibility Concerns

    Zimmer Biomet is recalling 412 units of ZCA All Poly Acetabular Cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.

    Product
    ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, 10 degree inclined face, O.D. Cup with Spacers, 59 mm Number: 00-8065-656-32
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0363-2021·2020-11-11

    Zimmer Biomet Recalls Acetabular Hip Cup Components Due to Sterilant Concerns

    Zimmer Biomet is recalling 412 units of ZCA All Poly Acetabular Cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.

    Product
    ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, 10 degree inclined face, O.D. Cup with Spacers, 49 mm Number: 00-8065-646-22
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0337-2021·2020-11-11

    Zimmer Biomet Recalls Acetabular Hip Cups Due to Sterilant Biocompatibility Concerns

    Zimmer Biomet is recalling 412 acetabular hip cup components because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.

    Product
    ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, Neutral, O.D. Cup with Spacers, 53 mm Item Number: 00-8065-550-22
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0395-2021·2020-11-11

    Zimmer Biomet Recalls Hip Prosthesis Components Due to Sterilant Biocompatibility Concerns

    Zimmer Biomet is recalling 412 units of ZCA All Poly Acetabular Cups because the hydrogen peroxide sterilant used was not evaluated for biocompatibility, posing a potential risk of adverse tissue reactions.

    Product
    ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, Snap-In O.D. Cup with Spacers, 57 mm Number: 00-8065-954-32
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0418-2021·2020-11-11

    Angiodynamics 5F Micro-Introducer Kits Recalled for Incorrect Device Packaging

    Angiodynamics, Inc. is recalling 32 kits of 5F Standard Micro-Introducer Kits because they may contain a 4F Sheath/Dilator component instead of the correct device.

    Product
    Angiodynamics 5F Standard Micro-Introducer Kit - indicated for percutaneous introduction of a guidewire or catheter into the vascular system, Catalog Number: 06597035 UPN: H787065970355
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0311-2021·2020-11-11

    GE Healthcare Recalls Aestiva/5 MRI Anesthesia Systems Due to Flow Sensor Defect

    GE Healthcare is recalling two Aestiva/5 MRI Anesthesia Systems because flow sensors may have damaged tubes with small punctures or cuts.

    Product
    Aestiva/5 MRI Anesthesia System - Product Usage: The Aestiva/5 MRI Anesthesia System provides the functional feature set offered by the conventional Aestiva/5 to the clinician with the added ability to be used in the MR environment. Among those standard Aestiva/5 features is the…
    Category
    Medical Device
    Distribution
    36 states
  • ModerateFDA (Devices)·Z-0319-2021·2020-11-11

    Boston Scientific Recalls LATITUDE Programming Systems Due to Software Defect

    Boston Scientific is recalling eight Model 3300 LATITUDE Programming Systems because a software defect may cause EGM trace channels to display as a flat line during specific tests.

    Product
    Model 3300 LATITUDE Programming System with installed Model 3892 ALTRUA, INSIGNIA I, NEXUS I Software Support Application
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0402-2021·2020-11-11

    Microbiologics Recalls Klebsiella Pneumoniae Strain Due to Incorrect VIM-1 Status

    Microbiologics Inc is recalling 46 units of a Klebsiella pneumoniae strain because it is VIM-1 negative instead of the expected VIM-1 positive status.

    Product
    Catalog 02145P, Klebsiella pneumoniae derived from NCTC 13439 - Product Usage: intended to be used as controls to verify the performance of assays, reagents or media that are intended to be used in microbial testing for the detection and identification of a cultured…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0064-2021·2020-11-11

    Teligent Pharma Recalls Fluocinonide Ointment Due to Impurity

    Teligent Pharma is recalling Fluocinonide Ointment USP 0.05% due to out-of-specification impurity results.

    Product
    Fluocinonide Ointment USP 0.05%, packaged in: a) 15 gm tube, NDC 52565-0040-15, b) 30 gm tube, NDC 52565-0040-30 c) 60 gram tube, NDC 52565-0040-60, Rx only, Manufactured by: Teligent Pharma, Inc., Buena, New Jersey 08310
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0066-2021·2020-11-11

    Jubilant Recalls Subpotent Olanzapine Orally Disintegrating Tablets Nationwide

    Jubilant Cadista Pharmaceuticals is voluntarily recalling 23,616 blister packs of Olanzapine Orally Disintegrating Tablets, 5 mg, because the product was found to be subpotent.

    Product
    Olanzapine Orally Disintegrating Tablets, 5 mg, 30 count (3x10 unit dose) blister pack, Rx only, Manufactured by: Jubilant Generics, Ltd., Roorkee, India, Marketed by: Jubilant Cardista Pharmaceuticals, Inc., Salisbury, MD NDC 59746-0306-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·21024·2020-11-10

    Kohl's Recalls SONOMA Goods For Life Three-Wick Candles Due to Fire Hazards

    Kohl's is recalling approximately 512,000 SONOMA Goods For Life three-wick candles because high flames can ignite wax or break glass, posing fire and burn risks.

    Product
    SONOMA Goods For Life branded three-wick candles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·21028·2020-11-10

    Ring Recalls 2nd Generation Video Doorbells Due to Fire Hazard

    Ring is recalling approximately 350,000 2nd Generation Video Doorbells because incorrect installation screws can cause the battery to overheat, posing fire and burn risks.

    Product
    Ring Video Doorbells (2nd Generation)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V695000·2020-11-10

    2021 Winnebago Micro Minnie Trailers Undersized Axles Recall

    Winnebago is recalling certain 2021 Micro Minnie trailers equipped with undersized axles that may break under the vehicle's weight, potentially causing serious injury or death.

    Product
    WINNEBAGO — WINNEBAGO MICRO MINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V692000·2020-11-10

    Ford Recalls Explorer, Taurus, and Edge for Drive Axle Bracket Failure

    Ford is recalling 2014-2016 Explorer, 2014-2015 Taurus, and 2014 Edge vehicles because a front drive axle bracket may fail, risking loss of park function or motive power.

    Product
    FORD — FORD TAURUS, EXPLORER, EDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·21027·2020-11-10

    Sunjoy Oakmont LP Fire Pit Tables Recalled for Fire Hazard

    Sunjoy is recalling Oakmont LP fire pit tables sold at Big Lots because an incorrectly installed hose can melt and ignite, posing a fire hazard.

    Product
    Oakmont LP fire pit tables
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V694000·2020-11-10

    Land Rover Recalls 2019-2020 Discovery Models for Electrical Faults

    Jaguar Land Rover is recalling 2019-2020 Discovery vehicles because a loose battery ground stud may cause electrical power loss or vehicle shutdown while driving.

    Product
    LAND ROVER — LAND ROVER DISCOVERY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21025·2020-11-10

    Salsa Cutthroat Bicycles Recalled Due to Fork Crack Injury Hazard

    Quality Bicycle Products is recalling Salsa Cutthroat bicycles because the fork legs can crack or break, posing a fall hazard to riders.

    Product
    Salsa Cutthroat Bicycles and Forks
    Category
    Consumer Product
    Distribution
    Distributed nationwide