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. 2,661 recalls have been distributed to Arkansas in the last 12 months.
Showing 2541–2560 of 49,990 recalls
Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...
The Issue: A new motor/encoder and cable was introduced into instruments manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Hemodialysis Catheter Sport Pack. Radiopaque...
The Issue: Potential breach of sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Pack....
The Issue: Potential breach of sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...
The Issue: A new software update (v1.20) is introducing error codes for the Dxl 9000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision SI Chronic Hemodialysis Catheter Sport Pack. Radiopaque...
The Issue: Potential breach of sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane...
The Issue: Potential breach of sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision H Chronic Hemodialysis Catheter Sport Pack. Radiopaque...
The Issue: Potential breach of sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apo B Reagent Recalled by Beckman Coulter Ireland, Inc. Due to The product...
The Issue: The product Value Assignment Sheet (VAS) is used in calibration of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Ranger Irrigation Fluid Warming Set Recalled by 3M Company Due to Notice...
The Issue: Notice was issued to clarify flow rates related to the inlet fluid temperature.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical Plum Solos Recalled by ICU Medical, Inc. Due to Internal testing...
The Issue: Internal testing found that Plum Duo pumps with software version 1.1.1 have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical Plum Duo Recalled by ICU Medical, Inc. Due to Internal testing...
The Issue: Internal testing found that Plum Duo pumps with software version 1.1.1 have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Catalyst+ Product Name: C4D software used in conjunction...
The Issue: Software issue with scanning equipment that can results in the filed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endopath Echelon Vascular White Reload for Advanced Placement Tip (35mm...
The Issue: Firm has received an increase in reports regarding inadvertent instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tirofiban Hydrochloride Injection 12.5 mg/250 mL (50 mcg/mL) Recalled by...
The Issue: Out-of-Specification test results were obtained in at long term conditions...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tirofiban Hydrochloride Injection 5 mg/100 mL (50 mcg/mL) Recalled by Eugia...
The Issue: Out-of-Specification test results were obtained in at long term conditions...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Precision Sampling Set Recalled by Capnia Inc Due to Sampling set nasal...
The Issue: Sampling set nasal cannula used with End-Tidal Carbon Monoxide (ETCO)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOWER EXTREMITY Recalled by American Contract Systems, Inc. Due to Test...
The Issue: Test results for cast padding component included in procedure trays shows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Cathena Safety IV Catheter BD Multiguard Technology 18 GA x 1.25 IN...
The Issue: Due to a manufacturing defect IV catheter may have a hole in the septum,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Timolol Maleate Ophthalmic Solution USP Recalled by FDC Limited Due to...
The Issue: Defective Container: Unable to get the solution out of the bottle as the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: niCARdipine Hydrochloride Injection Recalled by American Regent, Inc. Due to...
The Issue: Lack of sterility assurance: Product leakage around the vial neck, which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.