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. 943 recalls have been distributed to Arkansas in the last 12 months.
Showing 43121–43140 of 49,990 recalls
Recalled Item: Fluoxetine Capsules Recalled by Legacy Pharmaceutical Packaging Due to...
The Issue: Chemical Contamination: The recalling firm received notice that their...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: etomidate injection Recalled by Agila Specialties Private Ltd. Due to...
The Issue: Presence of Particulate Matter: Potential for small black particles to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RaySearch Ray Station Radiation Therapy Treatment Planning System Recalled...
The Issue: RaySearch Laboratories has recalled "RaySearch Ray Station 2.0, 2.5, 3.0,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Healthcare G2 Clinical Access Mislabeled CDs for PN: 063-1829-11...
The Issue: Spacelabs has voluntarily recalled G2 Clinical Access Software CD because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT580/Discovery CT590RT scanners running software...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Device Name: ABX PENTRA ML Model/Part #(s): A11A01652 Lot/Serial #(s):...
The Issue: HORIBA Medical initiated this recall of all software versions of ABX PENTRA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL Recalled by Philips Medical Systems, Inc. Due to...
The Issue: Philips HeartStart XL may experience a power board failure causing failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate) transdermal system patch Recalled by Noven...
The Issue: Defective Delivery System: Out of Specification (OOS) results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Other Macaroon G'nache P'nache 5.3 oz. Manufactured and Distributed...
The Issue: Northern Valley Baking Company did not declare milk or soy on the allergen...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VerifyNow IIb/IIIa Test Recalled by Accumetrics Inc Due to Accumetrics is...
The Issue: Accumetrics is recalling the VerifyNow IIb/IIIa test because it may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Solar 8000M and Solar 8000i Patient Monitor software version...
The Issue: GE Healthcare has recently become aware of a potential safety issue with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...
The Issue: Chemical Contamination: Recall due to a customer complaint trend regarding...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...
The Issue: Chemical Contamination: Recall due to a customer complaint trend regarding...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Jalapeno Burger Seasoning Recalled by Elite Spice Inc. Due to Potential...
The Issue: Bulk spice for futher manufacturing may be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mexican Style Mild Chorizo Recalled by Elite Spice Inc. Due to Potential...
The Issue: Bulk spice for futher manufacturing may be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Jalapeno Nut Seasoning Recalled by Elite Spice Inc. Due to Potential...
The Issue: Bulk spice for futher manufacturing may be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Jalapeno Ground 40 Recalled by Elite Spice Inc. Due to Potential Salmonella...
The Issue: Bulk spice for futher manufacturing may be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chipotle Nut Seasoning Recalled by Elite Spice Inc. Due to Potential...
The Issue: Bulk spice for futher manufacturing may be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ole Hot Chorizo Seasoning Recalled by Elite Spice Inc. Due to Potential...
The Issue: Bulk spice for futher manufacturing may be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.