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. 2,591 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,591 in last 12 months

Showing 1538115400 of 49,990 recalls

Medical DeviceApril 30, 2021· Nico Corp.

Recalled Item: NICO Myriad-LX Illumination Pack: Mvriad-LX Illumination Pack. 11ga Recalled...

The Issue: (1) Updated IFU for the LX Illumination Packs: Warning - Avoid contact...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2021· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Synapse Cardiovascular (Synapse CV). Software Versions: 6.0 to 6.2.1 The...

The Issue: Software versions 6.0.4 to 6.2.1 using Advanced Reporting -possibility that...

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

Class II — Potential Health HazardOngoing
DrugApril 29, 2021· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 120 Thyroid Tablets Recalled by Acella Pharmaceuticals, LLC Due...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 29, 2021· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 30 Thyroid Tablets Recalled by Acella Pharmaceuticals, LLC Due to...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 29, 2021· Ascend Laboratories LLC

Recalled Item: Olmesartan Medoxomil Tablets Recalled by Ascend Laboratories LLC Due to...

The Issue: Presence of Foreign Tablet/Capsule

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

Class III — Low RiskOngoing
Refund
DrugApril 29, 2021· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 60 Thyroid Tablets Recalled by Acella Pharmaceuticals, LLC Due to...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 29, 2021· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 90 Thyroid Tablets Recalled by Acella Pharmaceuticals, LLC Due to...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 29, 2021· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 15 Thyroid Tablets Recalled by Acella Pharmaceuticals, LLC Due to...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 29, 2021· Lupin Pharmaceuticals Inc.

Recalled Item: Cefixime for Oral Suspension USP 100 mg/5mL Recalled by Lupin...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 29, 2021· Pepsico Inc

Recalled Item: Evolve Vanilla Bean Plant-Based Protein Shake Recalled by Pepsico Inc Due to...

The Issue: undeclared soy

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 29, 2021· Pepsico Inc

Recalled Item: Evolve Double Chocolate Plant-Based Protein Shake Recalled by Pepsico Inc...

The Issue: undeclared soy

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 29, 2021· Covidien, LP

Recalled Item: Adult-Pediatric Electrostatic Filter HME Recalled by Covidien, LP Due to The...

The Issue: The company was notified by their supplier of sterilization services for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Covidien, LP

Recalled Item: Mechanical Filter with Connector Small Recalled by Covidien, LP Due to The...

The Issue: The company was notified by their supplier of sterilization services for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic HY10L28R3 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic CB10Y89R10 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic CB10W64R1 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic CB10W63R1 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic BB8M63R5 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic BB10R94R6 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic CB7J98R7 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing