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 1581–1600 of 49,990 recalls
Recalled Item: Medline Kits: 1) VALVE PACK-LF Recalled by Medline Industries, LP Due to The...
The Issue: The kits contain certain lots of cannula products where the catheter may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venclose digiRF Generators Recalled by Bard Peripheral Vascular Inc Due to...
The Issue: Software version 3.35 of the Venclose digiRF Generator incorporates a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT EG6+ cartridge. List Number: 03P77-25. Recalled by Abbott Point Of...
The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT CG4+ cartridge (white). List Number: 03P85-25. Recalled by Abbott...
The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG4+ cartridge to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT CG8+ cartridge. List Number: 03P88-25. 510(k) numbers: K894914...
The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT EG7+ cartridge. List Number: 03P76-25. Recalled by Abbott Point Of...
The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hostess Ding Dongs CHOCOLATE CAKE WITH CREAMY FILLING 2.55 oz Recalled by...
The Issue: Mold. The firm noticed an increase in customer complaints. They conducted a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sulfamethoxazole and Trimethoprim Tablets Recalled by Northwind...
The Issue: Presence of a Foreign Substance: A specific lot of auxiliary polyester coil,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen Injection 1000 mg/100 mL (10 mg/mL) Recalled by Baxter...
The Issue: Discoloration
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvedilol Tablets USP Recalled by The Harvard Drug Group LLC dba Major...
The Issue: CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MST ArcDUO 9mm Recalled by MicroSurgical Technology Inc Due to An ophthalmic...
The Issue: An ophthalmic knife has a suction set (not direct patient-contacting), which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Automated Impella Controller (AIC) with the below brands and product...
The Issue: Specific Automated Impella Controllers (AICs) that have a Pump Driver...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: READYPREP PVP Recalled by Medline Industries, LP Due to Subpotent drug
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Vacuette Product Name: 8 ml CAT Serum Separator Recalled by...
The Issue: Some of the Vacuette¿ CAT Serum Separator Clot Activator tubes were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.