State

Arkansas product recalls

73,096 recalls have nationwide distribution and so reach Arkansas. 5,542 additional recalls listed Arkansas specifically in their distribution scope.

What the numbers show

Total: 5,542
Critical: 1,029
Severe: 1,222
Most recent: 2026-09-23

Of the 5,542 recalls naming Arkansas we have scored against our rubric, 1,029 (19%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,222 (22%) are Severe.

Which agencies issued them

These figures cover only the 5,542 recalls whose distribution notice names Arkansas specifically. The 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9126–9150 of 78638

HighFDA (Devices)·Z-0496-2025·2024-11-27
Siemens Atellica CH Cuvette Segment manufacturing defect may impact lab test accuracy
Manufacturing defects in Siemens Atellica CH Cuvette Segments may cause inaccurate laboratory test results for seven analytes across 9,729 units.
Product
Siemens Atellica CH Reaction Ring Cuvette Segment-has cuvettes that contain and incubate the sample reaction volumes and present them to each processing step. Siemens Material Number(SMN): 11099326 All lots starting with N15 or 15 are expected to have the defect.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0141-2025·2024-11-27
Great Value Cinnamon Rolls Recalled for Plastic Contamination Nationwide
The JM Smucker Company is recalling Great Value Cinnamon Rolls nationwide due to possible plastic pieces in the product. Consumers should not consume affected units.
Product
Great Value Cinnamon Rolls 16.5oz UPC 078742201160, 12 retail units per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0471-2025·2024-11-27
Injection Needles Recalled for Manufacturing Debris Blocking Medication Flow
Hobbs Medical is recalling Posi-Stop Injection Needles due to manufacturing debris inside the needle shaft that blocks medication flow. The affected lot was distributed across multiple US states and Canada.
Product
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4716
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0476-2025·2024-11-27
FDA Recalls Posi-Stop Injection Needles Due to Manufacturing Debris
Hobbs Medical is recalling Posi-Stop Injection Needles (25 gauge) because some units contain debris in the needle shaft that blocks injection solution flow.
Product
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4723
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0486-2025·2024-11-27
Acrobat-i Vacuum Stabilizer System Recalled for Sterile Barrier Compromise
Maquet Cardiovascular is recalling approximately 33,823 units of the Acrobat-i Vacuum Stabilizer System due to manufacturing deviations that compromised the sterile barrier. Sterility cannot be assured for the 2-year shelf life.
Product
Acrobat-i Vacuum Stabilizer System. Model Number C-OM-10000Z
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0050-2025·2024-11-27
Guaifenesin Dextromethorphan Syrup Recalled for Failed Quality Specifications
Major Pharmaceuticals has recalled Guaifenesin Dextromethorphan Syrup due to failed impurity and degradation specifications. Three lot numbers were distributed nationwide.
Product
Guaifenesin Dextromethorphan Syrup, 100 mg/10mg per 5 mL, Major Pharmaceuticals 8401 Bearing Drive, Suite 100, Indianapolis, IN, 46268, NDC 0904-7134-70
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0475-2025·2024-11-27
Posi-Stop 25-Gauge Injection Needles Recalled for Manufacturing Debris Blockage
Hobbs Medical is recalling Posi-Stop 25-Gauge injection needles because some units contain manufacturing debris that blocks the needle's inner diameter, preventing injection solutions from flowing properly.
Product
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4722
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0054-2025·2024-11-27
Ramipril Capsule Medication Recalled Over Unapproved Vendor Manufacturing Deviations
Lupin Pharmaceuticals is recalling 357,414 bottles of Ramipril 10 mg capsules due to CGMP deviations where the active pharmaceutical ingredient was sourced from an unapproved vendor. The affected product was distributed to 30 wholesalers with potential nationwide distribution.
Product
RAMIPRIL — RAMIPRIL (RAMIPRIL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0049-2025·2024-11-27
Guaifenesin-Dextromethorphan Cough Syrup Recalled for Failed Impurity Specifications
Major Pharmaceuticals is recalling Guaifenesin Dextromethorphan Syrup nationwide for specific lots that failed to meet impurity and degradation specifications. Consumers should contact their pharmacist if they possess affected lots.
Product
Guaifenesin Dextromethorphan Syrup, 200 mg/20mg per 10 mL, Major Pharmaceuticals 8401 Bearing Drive, Suite 100, Indianapolis, IN, 46268, NDC 0904-7135-72
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0481-2025·2024-11-27
CAIRE FreeStyle Comfort portable oxygen concentrator battery recharge failure
Caire Inc. is recalling 26 CAIRE FreeStyle Comfort portable oxygen concentrators due to potential battery recharge failure. Affected units identified by serial number may not charge properly.
Product
CAIRE FreeStyle Comfort portable oxygen concentrator, model #AS200-2.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0497-2025·2024-11-27
Philips Vue PACS Diagnostic Viewer Software Recall for Calculation Errors
Philips is recalling Vue PACS Diagnostic Viewer software versions 12.1.5 to 12.2.8.454 because a defect may cause incorrect ischemic map calculations, potentially leading to misdiagnosis.
Product
Vue PACS Diagnostic Viewer with Vue PACS client 12.1.5 to 12.2.8.454 software Model Number: 1149418 Intended use is to provide completely scalable local and wide area PACS (Picture Archiving and Communication System) solutions for hospital and related institutions/sites.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0485-2025·2024-11-27
Acrobat SUV Vacuum Stabilizer System Sterile Barrier Compromise Recall
Maquet Cardiovascular is recalling the Acrobat SUV Vacuum Stabilizer System (Model C-OM-9000Z) due to manufacturing deviations that compromise the sterile barrier. Sterility cannot be assured during the 2-year shelf life, affecting approximately 10,778 units.
Product
Acrobat SUV Vacuum Stabilizer System, ST. Model Number C-OM-9000Z
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0472-2025·2024-11-27
Posi-Stop Injection Needle Recalled Due to Manufacturing Debris Blockage
Hobbs Medical is recalling Posi-Stop Injection Needles (23 Gauge, Lot H11-23-057) because some units contain manufacturing debris that blocks the needle opening, preventing injection solutions from flowing properly.
Product
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4721
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0052-2025·2024-11-27
FDA recalls Ramipril 2.5 mg capsules for manufacturing control deviations
Lupin Pharmaceuticals is recalling Ramipril 2.5 mg capsules after sourcing the active ingredient from an unapproved vendor. Approximately 112,770 bottles were distributed to wholesalers nationwide.
Product
RAMIPRIL — RAMIPRIL (RAMIPRIL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0473-2025·2024-11-27
Posi-Stop Injection Needles recalled for manufacturing debris blockage
Hobbs Medical is recalling Posi-Stop Injection Needles due to manufacturing debris that can block needle flow. Some units may contain debris in the inner sheath that prevents injection solutions from functioning properly.
Product
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4704
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0474-2025·2024-11-27
Posi-Stop Injection Needles Recalled Due to Manufacturing Debris Blocking Injection Flow
Hobbs Medical recalls Posi-Stop injection needles because manufacturing debris can block the needle, preventing injection solutions from flowing properly. Affected units were distributed across multiple US states and Canada.
Product
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4718
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0488-2025·2024-11-27
EnChroma Safety Glasses recalled for defective impact protection
EnChroma Inc recalls 53 units of safety glasses with Rx indoor lenses that fail impact safety standards, posing a risk of eye injury. Affected models include Martinez Cx1 Indoor Rx, Summit Indoor Rx, and Martinez Black Cx Rx.
Product
EnChroma Safety Glasses with Rx Indoor Universal Lenses: Martinez Cx1 Indoor Rx, SKU: Cx.PC.IN.MTZ.BK.Rx; Summit Indoor Rx, Cx.PC.IN.SUM.BK.Rx; Martinez Black Cx Rx, Cx-3.PC.PT.MTZ.BK.Rx
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0487-2025·2024-11-27
Ethicon Recalls Monocryl Sutures Due to Component Mix-Up
Ethicon, Inc. is recalling 16,524 units of Monocryl sutures because a manufacturing error may result in incorrect needle types, sizes, or suture lengths.
Product
MONOCRYL" (poliglecaprone 25) Suture REF Y936H MONOCRYL" Sutures are indicated for use in general soft tissue approximation and/or ligation, but not for use in cardiovascular and neurological tissues, microsurgery or ophthalmic surgery.
Category
Medical Device
Distribution
45 states
HighFDA (Devices)·Z-0484-2025·2024-11-27
Maquet Cardiovascular Recalls Acrobat-i Positioners Due to Sterility Concerns
Maquet Cardiovascular is recalling 14,338 Acrobat-i Positioners because manufacturing deviations compromised the sterile barrier, meaning sterility cannot be assured during the product's 2-year shelf life.
Product
Acrobat-i Positioner. Model Number C-XP-5000Z
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0057-2025·2024-11-27
Vitamin B1 Supplement Recalled for Blister Packaging Defect
Safecor Health is recalling certain Vitamin B1 supplements due to manufacturing defects where blister card-foils are separating from the blister cavity.
Product
Vitamin B1, 100 mcg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-108-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0059-2025·2024-11-27
Calcium Antacid (Calcium Carbonate) Recall Due to Blister Packaging Separation
Safecor Health recalls 791 boxes of Calcium Carbonate chewable tablets (Lot 24A0073) due to cGMP deviations where blister card-foils separated from blister cavities.
Product
CALCIUM ANTACID — CALCIUM ANTACID (CALCIUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0048-2025·2024-11-27
Triamcinolone Acetonide Cream USP Recalled for Out-of-Specification Potency Variance
Padagis is recalling 10,872 jars of Triamcinolone Acetonide Cream USP 0.025% nationwide because some jars contain subpotent or superpotent active ingredient levels. The defect was discovered during long-term stability testing.
Product
Triamcinolone Acetonide Cream USP, 0.025%, 1 LB (454 g) per jar, Rx Only, Manufactured By Padagis, Minneapolis, MN 55427. NDC: 45802-0063-05
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0498-2025·2024-11-27
Olympus Gastrointestinal Videoscope Drying Instructions Clarified
Olympus is recalling 1,749 GIF-1TH190 gastrointestinal videoscopes to clarify drying procedures in the instructions for use after human errors were identified during evaluation.
Product
Brand Name: EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190 Product Name: Olympus GIF-1TH190 Model/Catalog Number: GIF-1TH190 Software Version: N/A Product Description: This instrument is intended to be used with an Olympus video system center, light source, documentati
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0058-2025·2024-11-27
Aspirin 81 mg chewable tablets recalled due to packaging defect
Safecor Health, LLC is recalling 1,470 boxes of Aspirin 81 mg chewable tablets nationwide due to a manufacturing defect where blister card-foils are separating from the blister cavity.
Product
ASPIRIN — ASPIRIN (ASPIRIN 81 MG)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0056-2025·2024-11-27
Vitamin D3 Dietary Supplement Recalled for Packaging Defect
Safecor Health is recalling specific lots of Vitamin D3 25 mcg tablets due to a manufacturing defect where blister card-foils may separate from the blister cavity. No illnesses or injuries have been reported.
Product
Vitamin D3, 25 mcg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-104-01
Category
Drug
Distribution
Distributed nationwide