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. 949 recalls have been distributed to Arkansas in the last 12 months.
Showing 39441–39460 of 49,990 recalls
Recalled Item: Medical Device Exchange BAG Recalled by EXP Pharmaceutical Services Corp Due...
The Issue: EXP did not register as a medical device establishment, list the devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Device Exchange - GIA Auto Suture Loading Unit w/ Recalled by EXP...
The Issue: EXP did not register as a medical device establishment, list the devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Device Exchange FEMORAL CANAL TIP Recalled by EXP Pharmaceutical...
The Issue: EXP did not register as a medical device establishment, list the devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Device Exchange PhysioMesh Flexible Composite Mesh 10cm x 15cm...
The Issue: EXP did not register as a medical device establishment, list the devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Device Exchange X-SAW BLADE Recalled by EXP Pharmaceutical Services...
The Issue: EXP did not register as a medical device establishment, list the devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outer cardboard box labeling: Pinnacle Cure Sleeve Recalled by Sybron Dental...
The Issue: Cases of Cure Sleeve labeled with part number 4513, which fits 13mm tips,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMARTSET GHV Gentamicin Bone Cement. A self-curing Recalled by DePuy...
The Issue: One lot of SMARTSET GHV Gentamicin Bone Cement is partially agglomerated ....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoWrist One Vessel Sealer Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Intuitive Surgical has identified the potential for a certain, small portion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoWrist One Vessel Sealer Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Intuitive Surgical has identified the potential for a certain, small portion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Organic Sacha Inchi Powder Recalled by Sunfood Corportation Due to Sunfood...
The Issue: Sunfood is recalling Sacha Inchi Powder because it has the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: G7 Variant Elution Buffer HiS no. 1 (M) component of Recalled by Tosoh...
The Issue: The G7 Variant Elution Buffer HiS no. 1 (M) is incorrectly labeled with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dextroamphetamine Sulfate Extended-Release Capsules Recalled by Actavis...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CooperSurgical PESSARY KIT-CUBE#2 Recalled by CooperSurgical, Inc. Due to...
The Issue: Incorrect size printed on the Milex Pessary Kit packaging label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare DuraDiagnost X- Ray Recalled by Philips Medical Systems,...
The Issue: The system is designed to emit a beep upon termination of an exposure....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare DigitalDiagnost System X-Ray Recalled by Philips Medical...
The Issue: The system is designed to emit a beep upon termination of an exposure....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS SOMATOM Force with software version VA50A and /or VA50A_FP1 Recalled...
The Issue: Possibility of image artifacts during data acquisition when using Adaptive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo HX2 Temperature Management System provides temperature control of two...
The Issue: Malfunctioning mixing valve and loss of cooling and/or heating capability....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Antacid Liquid Regular Strength Antacid & Anti-Gas (Aluminum hydroxide 200...
The Issue: Microbial Contamination of Non-Sterile Products: Lots failed microbiological...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: UNCLE BEN'S(R) Ready Rice(R) NEW ORLEANS STYLE RED BEANS & RICE Recalled by...
The Issue: UNCLE BENS(R) Ready to Heat Pouches have the potential for containing metal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: UNCLE BEN'S(R) Ready Rice(R) ORIGINAL Recalled by Mars Food US Due to UNCLE...
The Issue: UNCLE BENS(R) Ready to Heat Pouches have the potential for containing metal...
Recommended Action: Do not consume. Return to store for a refund or discard.