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 1354113560 of 49,990 recalls

Medical DeviceDecember 8, 2021· R82 A/S

Recalled Item: R82 by ETAC Push Brace for High-Low Recalled by R82 A/S Due to The chrome...

The Issue: The chrome surface of the push brace can crack during use, potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2021· Technomed Europe

Recalled Item: Disposable Subdermal Needle Electrode Recalled by Technomed Europe Due to...

The Issue: There is a high risk of the blue hub detaching from the corkscrew needle,...

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

Class II — Potential Health HazardOngoing
DrugDecember 7, 2021· Direct Rx

Recalled Item: Diclofenac Sodium Topical Solution 1.5% Recalled by Direct Rx Due to...

The Issue: Defective Container: Leaking containers.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 7, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: Novalung Sensor Box (F30000163) a component of Novalung Console (F30000162)-...

The Issue: Error messages 206 (yellow) and 208 (red) technical failure, flow...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL UNITE REV STEM SZ 10 Product Code: 110010600 Recalled by DePuy...

The Issue: Stems may have an undersized spigot bore diameter therefore separating the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL UNITE STD STEM SZ 16 Product Code: 110016100 Recalled by DePuy...

The Issue: Stems may have an undersized spigot bore diameter therefore separating the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL UNITE STD STEM SZ 10 Part Number: 110010100 Recalled by DePuy...

The Issue: Stems may have an undersized spigot bore diameter therefore separating the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL UNITE STD STEM SZ 12 Product Code: 110012100 Recalled by DePuy...

The Issue: Stems may have an undersized spigot bore diameter therefore separating the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL UNITE REV STEM SZ 8 Part Number: 110008600 Recalled by DePuy...

The Issue: Stems may have an undersized spigot bore diameter therefore separating the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL UNITE STD STEM SZ 14 Product Code: 110014100 Recalled by DePuy...

The Issue: Stems may have an undersized spigot bore diameter therefore separating the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL UNITE STD STEM SZ 6 Part Number: 11000610 Recalled by DePuy...

The Issue: Stems may have an undersized spigot bore diameter therefore separating the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL UNITE STD STEM SZ 8 Part Number: 110008100 Recalled by DePuy...

The Issue: Stems may have an undersized spigot bore diameter therefore separating the...

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

Class II — Potential Health HazardOngoing
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Phenylephrine HCl/Tropicamide Recalled by Edge Pharma, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Dibutyl Squaric Acid Recalled by Edge Pharma, LLC Due to CGMP Deviations

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Edetate Disodium (EDTA) Recalled by Edge Pharma, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Edetate Disodium (EDTA) Recalled by Edge Pharma, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: MVASI Recalled by Edge Pharma, LLC Due to Lack of Assurance of Sterility

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Phenol Recalled by Edge Pharma, LLC Due to CGMP Deviations

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Profound-PE Dental Gel Recalled by Edge Pharma, LLC Due to CGMP Deviations

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Gemcitabine Recalled by Edge Pharma, LLC Due to Lack of Assurance of Sterility

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund