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. 2,641 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,641 in last 12 months

Showing 51215140 of 49,990 recalls

Medical DeviceJune 27, 2024· Boston Scientific Corporation

Recalled Item: Capio SLIM Suture Capturing Device Recalled by Boston Scientific Corporation...

The Issue: Some lots of Capio SLIM do not consistently catch the suture after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· Boston Scientific Corporation

Recalled Item: Capio SLIM Suture Capturing Device Recalled by Boston Scientific Corporation...

The Issue: Some lots of Capio SLIM do not consistently catch the suture after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· LINK BIO CORP

Recalled Item: LINK SymphoKnee Patella Sizing Template Recalled by LINK BIO CORP Due to The...

The Issue: The LinkSymphoKnee Patella Sizing Template was incorrectly labeled. The...

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

Class II — Potential Health HazardOngoing
DrugJune 26, 2024· Guru Inc.

Recalled Item: Infla-650 Herbal Dietary Supplement Recalled by Guru Inc. Due to Undeclared...

The Issue: Marketed without an approved NDA/ANDA: FDA analysis found product to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Sevelamer Carbonate for Oral Suspension 0.8g packets Recalled by Dr. Reddy's...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. Missing lot number and...

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

Class III — Low RiskOngoing
Refund
DrugJune 26, 2024· RemedyRepack Inc.

Recalled Item: Potassium Chloride Micro 10mEq K (750 mg) Extended Release Capsules Recalled...

The Issue: CGMP Deviations: Out of specification for dissolution

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2024· Equibal Inc

Recalled Item: Blemfree All Day Lotion (salicylic acid 0.5% w/w) Recalled by Equibal Inc...

The Issue: CGMP Deviations: Manufactured without following Current Good Manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2024· Medisca Inc.

Recalled Item: Budesonide Recalled by Medisca Inc. Due to CGMP Deviations and Presence of...

The Issue: CGMP Deviations and Presence of Particulate Matter: Glass

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 26, 2024· Siemens AG/Siemens Healthcare GmbH

Recalled Item: ARTIS is a family of dedicated angiography systems developed for Recalled by...

The Issue: A potential issue with ARTIS icono systems equipped with a small detector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2024· Siemens AG/Siemens Healthcare GmbH

Recalled Item: ARTIS is a family of dedicated angiography systems developed for Recalled by...

The Issue: A potential issue with ARTIS icono systems equipped with a small detector...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2024· Siemens AG/Siemens Healthcare GmbH

Recalled Item: ARTIS is a family of dedicated angiography systems developed for Recalled by...

The Issue: A potential issue with ARTIS icono systems equipped with a small detector...

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

Class II — Potential Health HazardOngoing
DrugJune 25, 2024· Amerisource Health Services LLC

Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Amerisource Health...

The Issue: Failed Dissolution Specifications

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 25, 2024· GLOBAL WIDGET LLC

Recalled Item: Hemp Bombs CBD Pain Freeze (menthol 4%) Recalled by GLOBAL WIDGET LLC Due to...

The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...

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

Class III — Low RiskOngoing
Refund
DrugJune 25, 2024· GLOBAL WIDGET LLC

Recalled Item: Nature's Script CBD Cryotherapy Pain Relief Roll on (menthol 4%) 200mg...

The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...

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

Class III — Low RiskOngoing
Refund
DrugJune 25, 2024· GLOBAL WIDGET LLC

Recalled Item: Hemp Bombs CBD Pain Freeze (menthol 4%) Recalled by GLOBAL WIDGET LLC Due to...

The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...

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

Class III — Low RiskOngoing
Refund
DrugJune 25, 2024· GLOBAL WIDGET LLC

Recalled Item: Hemp Bombs CBD Pain Freeze (menthol 4%) Recalled by GLOBAL WIDGET LLC Due to...

The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 25, 2024· UNIMAX MEDICAL SYSTEMS INC

Recalled Item: 1. Tech Medical Services Inc. Detachable Endo Retrieval Pouch Recalled by...

The Issue: The tube may fall into the surgical site during the grasping process.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2024· Preat Corp

Recalled Item: Multiple Digital Analog Products labeled as: NobelBiocare...

The Issue: Due to a manufacturing issue, the product has a out of specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2024· Thoratec LLC

Recalled Item: HeartMate 3 System Controllers provided within the following HeartMate 3...

The Issue: Left ventricular assist system controller UI membrane/screen may lift along...

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

Class II — Potential Health HazardOngoing
FoodJune 24, 2024· fgf brands, inc

Recalled Item: Bakeshop Chocolate Chip Muffin 4 count Recalled by fgf brands, inc Due to...

The Issue: Undeclared Walnut

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

Class II — Potential Health HazardOngoing
Refund