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. 2,628 recalls have been distributed to Arkansas in the last 12 months.
Showing 6561–6580 of 49,990 recalls
Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM Recalled by Howmedica Osteonics...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3 TRIATHLON CS INSERT NO 6 10 MM Recalled by Howmedica Osteonics Corp. Due...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3 TRIATHLON CS INSERT NO 3 10 MM Recalled by Howmedica Osteonics Corp. Due...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NO 3 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM Recalled by Howmedica Osteonics...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3 TRIATHLON CS INSERT NO 7 9 MM Recalled by Howmedica Osteonics Corp. Due...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3 TRIATHLON CS INSERT NO 6 11 MM Recalled by Howmedica Osteonics Corp. Due...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM Recalled by Howmedica Osteonics...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 with a Certeray generator-To perform image guidance in diagnostic...
The Issue: Generator may fail due to a potential short circuit in the Printed Circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 3 with a Certeray generator -To perform image guidance in diagnostic...
The Issue: Generator may fail due to a potential short circuit in the Printed Circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 5 with a Certeray generator-To perform image guidance in diagnostic...
The Issue: Generator may fail due to a potential short circuit in the Printed Circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune's Fix Recalled by Super Chill Products Due to Marketed without an...
The Issue: Marketed without an approved NDA/ANDA: Product contains tianeptine, a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mesalamine Extended-Release Capsules Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: Out of specification for dissolution.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Abbott Aveir Leadless Pacemaker Recalled by Abbott Medical Due to Their is a...
The Issue: Their is a potential that electromagnetic interference may cause leadless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyPoint Needle Recalled by Retractable Technologies, Inc. Due to The...
The Issue: The needle cannula of a retractable needle may detach from the needle holder...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omeprazole and Sodium Bicarbonate For Oral Suspension 40mg/1 Recalled by...
The Issue: Subpotent Drug: Out of specification for assay
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BVI Visitec Irrigation Handle (20/SP)- Intended to be fit with Recalled by...
The Issue: Pack and pouch label is missing the manufacturing and expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coffee 5 pound bags Recalled by House of Coffee Beans, Inc Due to potential...
The Issue: potential allergen contact with almonds, pecans and coconut.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RAM IT Recalled by Integrity Products Due to Undeclared Sildenafil
The Issue: Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: To the Moon Capsules Recalled by Integrity Products Due to Undeclared Sildenafil
The Issue: Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TING 1% Tolnaftate Athlete's Foot Spray Antifungal Spray Liquid Recalled by...
The Issue: Chemical Contamination; presence of benzene.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.