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. 1,033 recalls have been distributed to Arkansas in the last 12 months.
Showing 17301–17320 of 49,990 recalls
Recalled Item: Eye Itch Relief Recalled by Akorn, Inc. Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: pH-D Feminine Health Boric Acid Vaginal Suppositories Recalled by pH-D...
The Issue: Marketed without an Approved NDA/ANDA.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Biomet Comprehensive Reverse Shoulder Glenosphere Mini Baseplate with Taper...
The Issue: Product potentially being packaged without a taper adapter or baseplate. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Red-E Tablet Recalled by The Protein Shoppe Due to Marketed Without An...
The Issue: Marketed Without An Approved NDA/ANDA: product found to be tainted with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Spinning Spiros Closed Male Luer Recalled by ICU Medical, Inc. Due to...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Appx 1.7 ml Bag Spike w/Integrated Clave Recalled by ICU Medical, Inc. Due...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx 5.5 mL 20 Drop Admin Set w/Integrated Clave Drip Chamber...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spiros CLOSED MALE LUER w/RED CAP Recalled by ICU Medical, Inc. Due to...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 IN (13 cm) Appx 1.5 ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 76 cm (30") Appx 3.3 ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx 3.2 ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
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 Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 26 IN(66 cm) APPX 3.4ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 42 IN (107 cm) Appx 5.0 ml Recalled by ICU Medical, Inc. Due to Potential...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 31" (78 cm) Appx 3.4 ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinning Spiros Recalled by ICU Medical, Inc. Due to Potential for spinning...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3mL Syringe w/Spinning Spiros Recalled by ICU Medical, Inc. Due to Potential...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Medical Systems Corporation (OMSC) Evis Exera II Bronchovideoscope...
The Issue: The BF-Q180 bronchoscope is being recalled because it does not have a 510(k)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PermaFlo Flowable Composite 948 Shade: A2 - Product Usage: Recalled by...
The Issue: Due to a potential manufacturing issue (cross contamination), composite is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BenchMark ULTRA Advanced Staining System (IVD)- Material Number: 05342716001...
The Issue: Potential for Fluid leaks within the instruments, creating an electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.