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. 2,491 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,491 in last 12 months

Showing 2022120240 of 28,355 recalls

Medical DeviceApril 1, 2016· B Braun Medical Inc

Recalled Item: Dialog+ Hemodialysis machines: Dialog A + HE/BIC Product Code 710200L...

The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Reamer....

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Siemens Medical Solutions USA, Inc

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

The Issue: The Neonate Head protocol with the pediatric kernel Hp38 could result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· B Braun Medical Inc

Recalled Item: Dialog+ Hemodialysis machines: Conductivity Sensor (BIC) Item 3456103A The...

The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Plate Recalled...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· B Braun Medical Inc

Recalled Item: Dialog+ Hemodialysis machines: Dialog + 120 V DF+Adimea+WAN-BSL-BIC Product...

The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ray-Cot 1/2" x 1.5" : 60-08 Product Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Americot Blue 1/2" x 1.5" : 20-06S Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Cotton Balls-Strung 3/4" : 30-03 Product Usage: Recalled...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Cotton Balls-Strung 1/2" : 30-02 Product Usage: Recalled...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Policot 1/2" x 1/2" : 90-06 Product Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ultracot 15 mm x 15 mm (Glassine) by American Surgical...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ray-Cot 1/2" x 3" : 60-09 Product Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ultracot 70 mm x 10090 mm : Recalled by American Surgical...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Americot Blue 1/2" x 1/2" : 20-04S Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Americot Blue 3/8" x 2" : 20-26S Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Uniqcot 1/2" x 1/2" : 67-06 Product Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ultracot 5 mm x 13 mm (Glassine) by American Surgical...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ultracot 10 mm x 13 mm (Glassine) by American Surgical...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Delicot X 9 mm x 50 mm by American Surgical Company Due to...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing