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. 1,915 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
1,915 in last 12 months

Showing 2316123180 of 49,990 recalls

Medical DeviceFebruary 19, 2019· Smith & Nephew, Inc.

Recalled Item: smith&nephew SMF(TM) STANDARD OFFSET STIKTITE(TM) COATED STEM 12/14 TAPER -1...

The Issue: Complaints were received indicating that the outer label incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2019· Smith & Nephew, Inc.

Recalled Item: smith&nephew SMF(TM) HIGH OFFSET STIKTITE(TM) COATED STEM 12/14 TAPER -1H...

The Issue: Complaints were received indicating that the outer label incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2019· Avitus Orthopaedics, Inc.

Recalled Item: Avitus¿ Bone Harvester w/ Filter Insert - 8mm intended to Recalled by Avitus...

The Issue: Breach in the sterile barrier pouch may compromise sterility of the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2019· Avitus Orthopaedics, Inc.

Recalled Item: Avitus¿ Bone Harvester w/ Filter Insert - 5mm intended to Recalled by Avitus...

The Issue: Breach in the sterile barrier pouch may compromise sterility of the device.

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

Class II — Potential Health HazardOngoing
FoodFebruary 16, 2019· Concord Foods, LLC

Recalled Item: Concord Fresh Success Mild Salsa Seasoning Mix Recalled by Concord Foods,...

The Issue: Product contains undeclared allergen, milk.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 15, 2019· Heritage Pharmaceuticals, Inc.

Recalled Item: Etomidate Injection Recalled by Heritage Pharmaceuticals, Inc. Due to...

The Issue: Subpotent Drug.

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 15, 2019· Nature'S Path Foods Inc

Recalled Item: Nature's Path Organic Chocolate Choco Chimps Organic cereal. Net Wt....

The Issue: Gluten-free Cereals may contain undeclared gluten (wheat and barley).

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 15, 2019· Nature'S Path Foods Inc

Recalled Item: Nature's Path Organic Gorilla Munch Corn Puffs cereal. Net Wt. 10 oz (284 g)...

The Issue: Gluten-free Cereals may contain undeclared gluten (wheat and barley).

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 15, 2019· Nature'S Path Foods Inc

Recalled Item: Nature's Path Organic Cinnamon Jungle Munch cereal. Net Wt. 10 oz (284 g)...

The Issue: Gluten-free Cereals may contain undeclared gluten (wheat and barley).

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 15, 2019· Alere San Diego, Inc.

Recalled Item: Alere Cholestech LDX Analyzer Recalled by Alere San Diego, Inc. Due to The...

The Issue: The polarity of the output of power supply was reversed. Due to polarity of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2019· Covidien, PLC

Recalled Item: Covidien Force TriVerse electrosurgical device 10 cord-Intended as...

The Issue: Potential for the sterile packaging to be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· Bard Peripheral Vascular Inc

Recalled Item: PowerPort isp M.R.I. Implantable Port with Attachable 8F Polyurethane...

The Issue: Complaints received that products packaged with the incorrect introducer...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS with Option syngo DE Scan for Single Recalled by...

The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Confidence Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Edge Plus Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential risk of scans being aborted when using the optional Dual Spiral...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· ACell, Inc

Recalled Item: Gentrix Surgical Matrix Thick Recalled by ACell, Inc Due to The devices were...

The Issue: The devices were released from a lot for which one sample failed to meet the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2019· ACell, Inc

Recalled Item: Gentrix Surgical Matrix Thick Recalled by ACell, Inc Due to The devices were...

The Issue: The devices were released from a lot for which one sample failed to meet the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 13, 2019· Perrigo New York, Inc.

Recalled Item: Ciclopirox shampoo 1% Recalled by Perrigo New York, Inc. Due to Failed...

The Issue: Failed Degradation/Impurities Specifications: Out of specification related...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 13, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Lovastatin Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...

The Issue: CGMP Deviations: Finished product made with lovastatin drug substance that...

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

Class III — Low RiskOngoing
Refund