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. 1,856 recalls have been distributed to Arkansas in the last 12 months.
Showing 29841–29860 of 49,990 recalls
Recalled Item: 7 OZ PIZZA DOUGH BALL Recalled by Rich Products Corp Due to Potential E....
The Issue: The product was made with flour supplied by Ardent Mills who issued a recall...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ARTISAN CRUST PIZZA DOUGH 24/18 Recalled by Rich Products Corp Due to...
The Issue: The product was made with flour supplied by Ardent Mills who issued a recall...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dip Trio Mix Homemade Gourmet Dip Mix Net Wt. 2.9 Recalled by Phoenix Food,...
The Issue: Possible Salmonella contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ARTISAN-STYLE PIZZA DOUGH BALL distributed under the following sizes and...
The Issue: The product was made with flour supplied by Ardent Mills who issued a recall...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Large Stealth Chamber Recalled by Iba Dosimetry Due to When the Stealth...
The Issue: When the Stealth Chamber is used as a detector in relative dosimetry,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Hybrid Glenoid Base Large for the Comprehensive Shoulder System...
The Issue: Zimmer Biomet is conducting a voluntary recall for a single lot of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffmann LRF Safety Clip (Bone Transport Strut) Recalled by Stryker...
The Issue: Stryker is recalling Hoffmann LRF (Limb Reconstruction Frame) System Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venture RX Catheter Recalled by Vascular Solutions, Inc. Due to Vascular...
The Issue: Vascular Solutions, Inc. (VSI) is voluntarily removing all lots of Venture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clarke-Reich Laparoscopic Knot Pusher Recalled by Cook Inc. Due to...
The Issue: reprocessing instructions do not provide sufficient detailed information for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stamey Needle Recalled by Cook Inc. Due to reprocessing instructions do not...
The Issue: reprocessing instructions do not provide sufficient detailed information for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Introducer/Extractor Recalled by Cook Inc. Due to reprocessing...
The Issue: reprocessing instructions do not provide sufficient detailed information for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pereyra-Raz Ligature Carrier Recalled by Cook Inc. Due to reprocessing...
The Issue: reprocessing instructions do not provide sufficient detailed information for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pereyra Ligature Carrier 75 Recalled by Cook Inc. Due to reprocessing...
The Issue: reprocessing instructions do not provide sufficient detailed information for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StatLock¿ IV Premium Catheter Stabilization Device Recalled by Bard Access...
The Issue: StatLockTM IV Premium Catheter Stabilization Device may contain an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ETEST ETP32 (Ertapenem) Ref. 531640 Recalled by BioMerieux SA Due to False...
The Issue: False susceptible results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clozapine Tablets USP Recalled by Teva Pharmaceuticals USA Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Microalbumin Reagent Recalled by Beckman Coulter Inc. Due to Beckman Coulter...
The Issue: Beckman Coulter has confirmed that MA Reagent Lot M609458 may recover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brennen Skin Graft Mesher. Surgical instrument designed to expand skin...
The Issue: Sterilization validation failure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter...
The Issue: There is a possibility of a data acquisition disruption that may cause an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...
The Issue: There is a possibility of a data acquisition disruption that may cause an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.