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. 1,053 recalls have been distributed to Arkansas in the last 12 months.
Showing 15861–15880 of 49,990 recalls
Recalled Item: Endoskeleton TC Interbody System with Titan nanoLOCK Surface Technology...
The Issue: The shelf box identifies a small device actually contains a large device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Martin-Lewis Agar 20 Ea - Product Usage: use Recalled by Becton...
The Issue: Products show heavy growth of C. albicans after 24 hours of incubation due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sight OLO-E1/U1 Software and Operators Manual Software v2.56.1 Catalog #:...
The Issue: Discrepancy in labeling between the adult CBC ranges presented in the OLO...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinity Biotech Captia Measles IgM Kit Recalled by Clark Laboratories, Inc....
The Issue: Positive Control may run high out of its assigned ISR range and result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoskeleton TC Interbody System with Titan nanoLOCK Surface Technology...
The Issue: The shelf box identifies a small device actually contains a large device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Telmisartan Tablets Recalled by Alembic Pharmaceuticals Limited Due to...
The Issue: Labeling: Label-mixup
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Real Alkalized Water Recalled by Real Water, Inc. Due to FDA was notified of...
The Issue: FDA was notified of cases of acute liver failure after consumption of Real Water
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Real Alkalized Water Recalled by Real Water, Inc. Due to FDA was notified of...
The Issue: FDA was notified of cases of acute liver failure after consumption of Real Water
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Spinning Spiros Closed Male Luer - Product Usage: Recalled by ICU Medical,...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spiros" Closed Male Luer - Product Usage: provides Recalled by ICU Medical,...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 180 cm (71 IN)APPX 11.5ml Recalled by ICU Medical, Inc. Due to Due to...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinning Spiros Closed Male Luer Recalled by ICU Medical, Inc. Due to Due to...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OPTICHAMBER DIAMOND SPACER WITH LARGE MASK Item Number: 4742326 Recalled by...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 40" (102 cm) Appx. 4.8 ml Recalled by ICU Medical, Inc. Due to Due to...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCU-CHEK SMARTVIEW 100 TEST STRIPS Item Number: 4742862 Recalled by...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 35" (89 cm) Appx 3.9 ml Recalled by ICU Medical, Inc. Due to Due to molding...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinning Spiros¿ Closed Male Luer Recalled by ICU Medical, Inc. Due to Due...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx 3.3 mL Recalled by ICU Medical, Inc. Due to Due to molding...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 60mL Syringe w/Spinning Spiros Recalled by ICU Medical, Inc. Due to Due to...
The Issue: Due to molding defect, there is a potential that certain lots of spinning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AEROCHAMBER PLS W/MASK LRG BLU Item Number: 1496033 Recalled by Cardinal...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.