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. 2,617 recalls have been distributed to Arkansas in the last 12 months.
Showing 10881–10900 of 49,990 recalls
Recalled Item: CAIRE Liberator 20 Recalled by Caire, Inc. Due to An audit discovered some...
The Issue: An audit discovered some inconsistencies in weld penetration on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE Liberator 30 Recalled by Caire, Inc. Due to An audit discovered some...
The Issue: An audit discovered some inconsistencies in weld penetration on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE Liberator 45 Recalled by Caire, Inc. Due to An audit discovered some...
The Issue: An audit discovered some inconsistencies in weld penetration on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PAJUNK Continuous Epidural Tray Recalled by Pajunk Medical Systems, L.P. Due...
The Issue: The tray contains a 2ml ampule of 0.75% Marcaine Spinal in lieu of a 10ml...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORISE Gel Submucosal Lifting Agent--Indicated for use in gastrointestinal...
The Issue: ***Update12/13/22***:Product removal due to higher incidence of adverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORISE Gel Syringe Submucosal Lifting Agent Kits: indicated for use Recalled...
The Issue: ***Update12/13/22***:Product removal due to higher incidence of adverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORISE ProKnife Procedure Kits: indicated for use in gastrointestinal...
The Issue: ***Update12/13/22***:Product removal due to higher incidence of adverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Octreotide Acetate Injection 500 mcg/mL Recalled by Viatris Inc Due to...
The Issue: Presence of Particulate Matter: Product complaint for the presence of glass...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TASTYKAKE GLAZED CARAMEL APPLE PIE NET WT 4.5 OZ (128g) Recalled by Flowers...
The Issue: During an internal inspection the firm discovered that several products may...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TASTYKAKE GLAZED LEMON FLAVORED PIE NET WT 4.5 OZ (128g) Recalled by Flowers...
The Issue: During an internal inspection the firm discovered that several products may...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mrs. Freshley's Apple Fruit Pie NET WT 4.5 OZ (128g) Recalled by Flowers...
The Issue: During an internal inspection the firm discovered that several products may...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mrs. Freshley's Cherry Fruit Pie NET WT 4.5 OZ (128g) Recalled by Flowers...
The Issue: During an internal inspection the firm discovered that several products may...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TASTYKAKE GLAZED CHERRY PIE NET WT 4.5 OZ (128g) Recalled by Flowers Foods...
The Issue: During an internal inspection the firm discovered that several products may...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TASTYKAKE GLAZED APPLE PIE NET WT 4.5 OZ (128g) Recalled by Flowers Foods...
The Issue: During an internal inspection the firm discovered that several products may...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FERNO POWER X1 AMBULANCE COT- Item #0015807/UDI-DI 00190790002183 with 36V...
The Issue: Batteries could become unstable when not properly maintained and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifampin Capsules Recalled by Golden State Medical Supply Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Finished product exceeds the 5...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rifampin Capsules Recalled by Golden State Medical Supply Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Finished product exceeds the 5...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP...
The Issue: Due to an increase of confirmed latex deterioration complaints for arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fogarty Biliary Balloon Probes Model Number: 410235FP 410405FP 410236FP...
The Issue: Due to an increase of confirmed latex deterioration complaints for arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quinapril and Hydrochlorothiazide Tablets Recalled by Aurobindo Pharma USA...
The Issue: CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.