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. 1,875 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
1,875 in last 12 months

Showing 2764127660 of 49,990 recalls

DrugOctober 19, 2017· SCA Pharmaceuticals, LLC

Recalled Item: Calcium GLUCOnate 2 g added to 0.9% Sodium Chloride 50 mL Bag Recalled by...

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
DrugOctober 19, 2017· SCA Pharmaceuticals, LLC

Recalled Item: HYDROmorphone HCl 20 mcg / mL BUPIvacaine HCl 0.075% in Recalled by SCA...

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
DrugOctober 19, 2017· SCA Pharmaceuticals, LLC

Recalled Item: ROCuronium Bromide 10 mg per mL Recalled by SCA Pharmaceuticals, LLC Due to...

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
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 22701 Recalled by Datascope Corporation Due to The Better Bladder...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 22702 ECC W/HMOD 30000 Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 22300 Recalled by Datascope Corporation Due to The Better Bladder...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 27610 ECC PACK 3/8 Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 22301 Recalled by Datascope Corporation Due to The Better Bladder...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 33700 ECC 3/8" PACK Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: Adult ECC Pack BEQ-TOP 22300 Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BO-TOP 13901 RAPID RESPONSE Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: ECC Small - Respiratory BEQ-TOP 5210 Recalled by Datascope Corporation Due...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BO-TOP 20700 SMALL PATIENT 3/8 Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 5210 ECC Set - Respiratory Recalled by Datascope Corporation Due to...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 38900 ECC PACK Recalled by Datascope Corporation Due to The Better...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-T 25502 1/4 Better Bladder Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 49101 Childrens Large ECC Pack Recalled by Datascope Corporation Due...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: NICU ECC Pack BEQ-TOP 39202 Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BO-TOP 20705 SMALL PATIENT 1/4 Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 41201 ECC 3/8 PUMP PAC Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing