Product Recalls in Arkansas

Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,598 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,598 in last 12 months

Showing 1362113640 of 49,990 recalls

DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CariFree CTx4 GEl 5000 1.1% Neutral Sodium Fluoride Mint Recalled by Dental...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CTx36 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Dental Alliance Holdings LLC

Recalled Item: CTx26 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Akorn, Inc.

Recalled Item: Morphine Sulfate Oral Solution 100 mg per 5 mL (20 mg/mL) 30 mL bottles...

The Issue: Labeling: Missing Label

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Akorn, Inc.

Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by Akorn, Inc. Due to...

The Issue: Labeling: Missing Label

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugDecember 3, 2021· Gilead Sciences, Inc.

Recalled Item: Veklury (remdesivir) for injection Recalled by Gilead Sciences, Inc. Due to...

The Issue: Presence of Particulate Matter: investigation into a customer complaint...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
FoodDecember 3, 2021· Slayer Forever, LLC dba BUBS Naturals

Recalled Item: BUBS Naturals Fountain of Youth Formula Recalled by Slayer Forever, LLC dba...

The Issue: Supplement contains undeclared milk from MCT oil powder ingredient.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 3, 2021· Konica Minolta Healthcare Americas, Inc.

Recalled Item: ImagePilot Versions 1.92 and 1.93-software primarily facilitates processing...

The Issue: lmagePilot versions 1.92 and 1.93 paired with an AeroDR or Momentum Panel...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2021· Wright Medical Technology, Inc.

Recalled Item: Wright Medical Technology Inc. CHARLOTTE MTP Hex Screw Recalled by Wright...

The Issue: Incorrect product is contained in the packaging.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 2, 2021· Torrent Pharma Inc.

Recalled Item: Carbamazepine Tablets Recalled by Torrent Pharma Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 2, 2021· LivaNova USA, Inc.

Recalled Item: Vagus Nerve Stimulation (VNS) Therapy Leads Recalled by LivaNova USA, Inc....

The Issue: A manufacturing issue may cause the silicone tubing wall thickness of vagus...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2021· Natus Neurology DBA Excel Tech., Ltd. (XLTEK)

Recalled Item: IPELA FHD PTZ TILE KITS with Axis cameras used in Recalled by Natus...

The Issue: Tile kits that allow one to install and situate a video camera within a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 1, 2021· Torrent Pharma Inc.

Recalled Item: Telmisartan and Hydrochlorothiazide Tablets Recalled by Torrent Pharma Inc....

The Issue: Superpotent; Hydrochlorothiazide

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 1, 2021· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Michels Transport Medium Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Product stored incorrectly in temperature controlled setting instead of .

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2021· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: HARDY DIAGNOSTICS CatScreen Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Product stored incorrectly in temperature controlled setting instead of .

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2021· CELLTRION USA INC

Recalled Item: Celltrion DiaTrust COVID-19 Ag Rapid Test Recalled by CELLTRION USA INC Due...

The Issue: The European version of the DiaTrust COVID-19 Ag Rapid Test is not approved...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2021· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Premier Rotaclone Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Product stored incorrectly in temperature controlled setting instead of .

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH ¿2-Microglobulin (B2M) -M) Assay for in vitro diagnostic...

The Issue: ¿2 Microglobulin (B2M) Reagent Lot 211446 Bias with Quality Control and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2021· Maquet Cardiovascular, LLC

Recalled Item: Hemashield Gold Knitted Bifurcated Recalled by Maquet Cardiovascular, LLC...

The Issue: There is a probable mislabeling of product. A Hemashield Platinum Woven...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugNovember 30, 2021· Teligent Pharma, Inc.

Recalled Item: Lidocaine Hydrochloride Recalled by Teligent Pharma, Inc. Due to Superpotent...

The Issue: Superpotent Drug: Minimally superpotent

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund