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. 2,623 recalls have been distributed to Arkansas in the last 12 months.
Showing 7301–7320 of 28,355 recalls
Recalled Item: InPen Diabetes Management App Recalled by Companion Medical, Inc. Due to...
The Issue: Diabetes management app may crash immediately upon opening, while using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R&D CBC-3D Hematology Control: (1) CBC-3D Normal Pack Hematology Control...
The Issue: For one lot of CBC-3D Hematology Control, the Normal Level may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis Angiographic Catheter Extensions. Used to transport fluid from the...
The Issue: There is a potential for separation at the male connector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-c Anesthesia System (Product Code 6887700) Flow-e Anesthesia System...
The Issue: The power backup battery, under certain conditions, may exhibit reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Action INDUSTRIES INC. Port a Cath Kit Recalled by Medical Action...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests Japan...
The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests (600T)-...
The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests OUS...
The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HF Resection Electrodes Recalled by Olympus Corporation of the Americas Due...
The Issue: An incompatible HF cable may be packaged with the HF Resection Electrodes....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VADER Pedicle System Torque Wrench Recalled by Icotec Ag Due to During...
The Issue: During internal testing (at manufacturer site) of two torque wrench devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynCardia Total Artificial Heart System (70CC): 500101-001 SynCardia Total...
The Issue: Due to tears reported tears in the cannula due to wear and tear stress.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...
The Issue: Medical and surgical procedure trays and kits underwent certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STRADIS HEALTHCARE Recalled by Stradis Medical, LLC dba Stradis Healthcare...
The Issue: Medical and surgical procedure trays and kits underwent certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STRADIS HEALTHCARE Recalled by Stradis Medical, LLC dba Stradis Healthcare...
The Issue: Medical and surgical procedure trays and kits underwent certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...
The Issue: Medical and surgical procedure trays and kits underwent certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STRADIS HEALTHCARE Recalled by Stradis Medical, LLC dba Stradis Healthcare...
The Issue: Medical and surgical procedure trays and kits underwent certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...
The Issue: Medical and surgical procedure trays and kits underwent certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...
The Issue: Medical and surgical procedure trays and kits underwent certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STRADIS HEALTHCARE Recalled by Stradis Medical, LLC dba Stradis Healthcare...
The Issue: Medical and surgical procedure trays and kits underwent certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...
The Issue: Medical and surgical procedure trays and kits underwent certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.