Product Recalls in Maine
Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,355 recalls have been distributed to Maine in the last 12 months.
Showing 31041–31060 of 48,770 recalls
Recalled Item: X-Celerator Hydrophilic Exchange Guidewire Catalog No. 103-0601-300...
The Issue: Delamination and detachment of the PTFE (polytetrafluoroethylene) coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arsenal Spinal Fixation System Recalled by Alphatec Spine, Inc. Due to...
The Issue: Alphatec Spine is recalling the Arsenal Spinal Fixation System Set Screw due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Antibacterial Hydrophilic Intermittent Catheter Recalled by C.R....
The Issue: Misbranding; the product labeled as an Antibacterial Hydrophilic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Marathon Flow Directed Micro Catheter Recalled by Micro Therapeutics Inc,...
The Issue: Delamination and detachment of the PTFE (polytetrafluoroethylene) coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur¿ Vitamin D Total Assay SMN SMN 10699533 (500 test)...
The Issue: Vitamin D Total- Change in Correlation Between Serum and Plasma Specimen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur¿ Vitamin D Total Assay SMN 10699201 (100 test)...
The Issue: Vitamin D Total- Change in Correlation Between Serum and Plasma Specimen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harmony Insight Diagnostic Monitor Support System - 100 Spring Arm Recalled...
The Issue: The Drager Pendula spring arm device has a set of screws located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Professional Botanicals MealPlex (756 grams) and Veo Natural Pearl 3.0...
The Issue: Professional Botanicals announces a voluntary field action for MealPlex and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Tina-Quant Hemoglobin A1c Gen. 2 Hemoglobin A1c test Catalog number Recalled...
The Issue: Roche Diagnostics has confirmed elevated QC and patient sample recovery for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBAS INTEGRA 800 Tina-Quant Hemoglobin A1cDX Gen.2 Hemoglobin A1cDX test...
The Issue: .Roche Diagnostics has confirmed elevated QC and patient sample recovery for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Best Practices kits containing certain production lots of Clearify...
The Issue: Product sterility is compromised due to breach of the sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Normal Saline Flush 0.9% USP Sodium Chloride Injection Syringe Recalled by...
The Issue: Potential contamination with B. cepacia.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Clearify Visualization System Item Code: 21-345 Intended to be...
The Issue: Product sterility is compromised due to breach of the sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm Reaming Rod W/Ball Tip 650 mm Recalled by Synthes (USA) Products LLC...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extraction Hook - Sterile for TI Cannulated Nails Recalled by Synthes (USA)...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.0 mm Reaming Rod/950 mm w/straight Ball Tip Recalled by Synthes (USA)...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.0 mm Reaming Rod/950 mm Recalled by Synthes (USA) Products LLC Due to The...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TBS iNsight Version v.3.0.1 Product Usage: TBS iNsight is a Recalled by...
The Issue: The FRAX adjusted for TBS values are not correct when: The FRAX feature is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model 37751 Recharger Product Usage: The Medtronic 37751 Recharger is...
The Issue: Medtronic has identified an increased number of complaints from customers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm TI Calibrated Reaming Rod 850 mm Recalled by Synthes (USA) Products...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.