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. 2,635 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,635 in last 12 months

Showing 62816300 of 49,990 recalls

FoodMarch 7, 2024· John B. Sanfilippo & Son Inc.

Recalled Item: Great Value Honey Roasted Cashews Recalled by John B. Sanfilippo & Son Inc....

The Issue: undeclared milk and coconut

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 7, 2024· Stonewall Kitchen, LLC

Recalled Item: Stonewall Kitchen Cinnamon Sugar Doughnut Mix Recalled by Stonewall Kitchen,...

The Issue: Product contains undeclared wheat.

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 7, 2024· Teva Pharmaceuticals USA, Inc

Recalled Item: Tri-Lo-Sprintec (norgestimate and ethinyl estradiol) tablets USP - triphasic...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 7, 2024· Olympus Corporation of the Americas

Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...

The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2024· Olympus Corporation of the Americas

Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...

The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2024· Olympus Corporation of the Americas

Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...

The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...

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

Class II — Potential Health HazardOngoing
FoodMarch 6, 2024· Colonna Brothers Inc.

Recalled Item: Supreme Tradition brand and Marcum brand ground cinnamon. Packaged in...

The Issue: Elevated lead levels in cinnamon

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 6, 2024· B. Braun Medical Inc

Recalled Item: Potassium Chloride for Injection Concentrate USP Recalled by B. Braun...

The Issue: Lack of assurance of sterility: pinholes, within the blue label characters...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 6, 2024· Outset Medical, Inc.

Recalled Item: Tablo Hemodialysis System Recalled by Outset Medical, Inc. Due to...

The Issue: Hemodialysis System, pre and post dialyzer peroxide-cured silicone tubing,...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 6, 2024· Artivion, Inc

Recalled Item: CryoValve SG Cryopreserved Pulmonary Human Heart Valve Recalled by Artivion,...

The Issue: The blood cultures performed as part of the organ donation process were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Microbiologics Inc

Recalled Item: KWIK-STIK Rhizopus stolonifer (+) derived from ATCC 6227b Recalled by...

The Issue: The positive control material (Rhizopus stolonifer) within the KWIK-STIK...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe Constrained Humeral Liner: Item Numbers: a) 320-40-10...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe REVERSE SHOULDER Recalled by Exactech, Inc. Due to The...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe Humeral Liner: Item Numbers: a) 320-40-00 Recalled by...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe CAGE GLENOID Recalled by Exactech, Inc. Due to The...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe CAGE GLENOID Recalled by Exactech, Inc. Due to The...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing