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. 2,558 recalls have been distributed to Arkansas in the last 12 months.
Showing 14141–14160 of 28,355 recalls
Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical Inc Due to...
The Issue: Failure of Universal Surgical Manipulators due to a high friction points,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution Recalled by NxStage Medical, Inc. Due to Mislabeling
The Issue: Certain lots were mislabeled with incorrect product number.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution Recalled by NxStage Medical, Inc. Due to Mislabeling
The Issue: Certain lots were mislabeled with incorrect product number.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straight Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straight Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Curved Intraluminal Stapler Recalled by Ethicon Endo-Surgery Inc...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Curved Intraluminal Stapler Recalled by Ethicon Endo-Surgery Inc...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straight Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curved Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to The...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Curved Intraluminal Stapler Recalled by Ethicon Endo-Surgery Inc...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straight Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curved Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to The...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curved Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to The...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Curved Intraluminal Stapler Recalled by Ethicon Endo-Surgery Inc...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curved Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to The...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProACT Implantation Instrument Set Recalled by Uromedica Inc. Due to...
The Issue: Potential issue with the manufacture and inspection of U-channel sheaths in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neurovascular Recalled by Stryker Neurovascular Due to The firm has...
The Issue: The firm has become aware of a potential problem that their Catheters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neurovascular Recalled by Stryker Neurovascular Due to The firm has...
The Issue: The firm has become aware of a potential problem that their Catheters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MaxZero Extension Sets with Needle-less Connector Recalled by Becton...
The Issue: BD has decided to initiate a voluntary recall due to a confirmed complaint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cepheid Xpert MRSA/MRSA NxG Control Panel (Catalog #8195) UDI:...
The Issue: Product with incorrect shelf life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.