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. 1,875 recalls have been distributed to Arkansas in the last 12 months.
Showing 28261–28280 of 49,990 recalls
Recalled Item: 159" (404 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 88" (224 cm) Y-Type Blood Set w/200 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 121" (307 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 134" (340 cm) Y-Type Admin Set w/170 Micron Blood Filter Recalled by ICU...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 32" (81 cm) Appx 4.4 mL Blood Set w/20 Drop 200 Micron Filter Recalled by...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 132" (335 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 94" (239 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 147" (373 cm) Bifuse Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 98" (249 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Friendly Farms Key Lime Crunch Tilts Greek Lowfat Yogurt Recalled by...
The Issue: Recalling Friendly Farms Key Lime Crunch Tilts because it may contain...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Aldi liveGfree Gluten Free Classic Soft White Hamburger Buns Recalled by...
The Issue: Undeclared eggs
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AIRO Mobile CT System Recalled by Brainlab AG Due to Risk of unintended...
The Issue: Risk of unintended motion while the AIRO system is in transport mode.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Famotidine USP 20 mg Recalled by PD-Rx Pharmaceuticals, Inc. Due to Failed...
The Issue: Failed Tablet/Capsule Specification: out of specification for tablet weight.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: A.T.S. 2200TS Tourniquet Systems Recalled by Zimmer Surgical Inc Due to...
The Issue: Updated on-device label and 3 pages of an updated Operator/Service Manual....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iVue 500 with iScan Recalled by Optovue, Inc. Due to FDA determined that a...
The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iFusion Recalled by Optovue, Inc. Due to FDA determined that a 510(k) is...
The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VCLAS (Visualase Cooled Laser Ablation System) Part Number: 9735559...
The Issue: The VCLAS 3mm, 10mm, and 15mm tip devices were not appropriately tested for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iVue with Normative Database Recalled by Optovue, Inc. Due to FDA determined...
The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.T.S. 4000TS Tourniquet Systems Recalled by Zimmer Surgical Inc Due to...
The Issue: Updated on-device label and 3 pages of an updated Operator/Service Manual....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Concorde Lift Torque Limiting Handle. Must be used with supplemental...
The Issue: Potential for Intra-operative breakage of driver tips
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.