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 28201–28220 of 49,990 recalls
Recalled Item: Major Ferrous Drops Recalled by The Harvard Drug Group Due to The...
The Issue: The distribution firms Leader Brand, Major Pharmaceuticals, and The Harvard...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cell Saver Elite Processing Kit Recalled by Haemonetics Corporation Due to...
The Issue: Haemonetics has received isolated reports that in some cases the 70ml...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Saver 5/5+ Bowl Set Recalled by Haemonetics Corporation Due to...
The Issue: Haemonetics has received isolated reports that in some cases the 70ml...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The OriGen Reinforced Dual Lumen catheter (RDLC) is a duel Recalled by...
The Issue: Two users have reported to OriGen that a VV28F OriGen Reinforced Dual Lumen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemosll ReadiPlasTin (20 ml Size) Recalled by Instrumentation Laboratory Co....
The Issue: Instrumentation Laboratory Co. received customer reports of performance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JANUS & JANUS G3 Automated Workstation is an automated programmable Recalled...
The Issue: We have become aware through internal testing that JANUS and Janus G3...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource(R) Kits (custom surgical/procedural kits): The standard and custom...
The Issue: The firm manufactured and distributed Presource(R) kits which contained BD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versys 6 inch Beaded Full Coat Plus Hip Prosthesis. Labeled Recalled by...
The Issue: The products being recalled exceeded the weight previously tested leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Segmental System Recalled by Zimmer Biomet, Inc. Due to The products...
The Issue: The products being recalled exceeded the weight previously tested leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NATURAL HERBAL COFFEE AMPT Recalled by The Ampt Life, LLC Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 115" (292 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: 143" (363 cm) 20 Drop Y-Type Blood Set w/200 Micron 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: 125" (318 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: Central Venous Catheter Set Triple Lumen Polyurethane Recalled by Cook Inc....
The Issue: Central venous catheters may not fit over guide wire potentially causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 99" (251 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: Central Venous Catheter Tray Triple Lumen Polyurethane Recalled by Cook Inc....
The Issue: Central venous catheters may not fit over guide wire potentially causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 164" (417 cm) 20 Drop Y-Type Blood Admin Set w/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: Spectrum Central Venous Catheter Tray Minocycline/Rifampin Antibiotic...
The Issue: Central venous catheters may not fit over guide wire potentially causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 137" (348 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: 175" (445 cm) Y-Type Blood 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.