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. 1,911 recalls have been distributed to Arkansas in the last 12 months.
Showing 23861–23880 of 49,990 recalls
Recalled Item: NxStage PureFlow B Solution-RFP-402 Recalled by NxStage Medical, Inc. Due to...
The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution-RFP-400 Recalled by NxStage Medical, Inc. Due to...
The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution-RFP-RFP-456 Recalled by NxStage Medical, Inc....
The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution-RFP-401 Recalled by NxStage Medical, Inc. Due to...
The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution-RFP-RFP-454 Recalled by NxStage Medical, Inc....
The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution-RFP-404 Recalled by NxStage Medical, Inc. Due to...
The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution-RFP-406 Recalled by NxStage Medical, Inc. Due to...
The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution-RFP-403 Recalled by NxStage Medical, Inc. Due to...
The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trader Joe's Tomato & Basil Hummus Dip Recalled by Bakkavor Foods USA, Inc....
The Issue: Hummus was recalled due to potential Salmonella and/or Listeria...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Trader Joe's Hummus quartet Recalled by Bakkavor Foods USA, Inc. Due to...
The Issue: Hummus was recalled due to potential Salmonella and/or Listeria...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The PLEX Elite 9000 Recalled by Carl Zeiss Meditec, Inc. Due to Under...
The Issue: Under certain fault conditions, the existing design may expose the operator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Argon Medical Devices Vascuclamp Recalled by Argon Medical Devices, Inc...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices TRI-JECT Recalled by Argon Medical Devices, Inc Due to...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Argon Medical Devices Double Female LL Adapter Recalled by Argon Medical...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices Double Male LL Adapter Recalled by Argon Medical...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices AHD Luer Lock Cap Recalled by Argon Medical Devices,...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices Hemostasis Valve Recalled by Argon Medical Devices,...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices Septishield II Recalled by Argon Medical Devices, Inc...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices Plugs Recalled by Argon Medical Devices, Inc Due to...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Argon Medical Devices Stopcocks Recalled by Argon Medical Devices, Inc...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.