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. 2,492 recalls have been distributed to Maine in the last 12 months.
Showing 12501–12520 of 27,655 recalls
Recalled Item: Healix Knotless ADV BR 4.75 Suture Anchor Recalled by DePuy Mitek, Inc., a...
The Issue: Specific product codes and lots of the Mitek HEALIX ADVANCE" Knotless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Healix Knotless ADV BR 5.5 Suture Anchor Recalled by DePuy Mitek, Inc., a...
The Issue: Specific product codes and lots of the Mitek HEALIX ADVANCE" Knotless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Site~Rite 8 Ultrasound Systems-intended for diagnostic ultrasound imaging of...
The Issue: The indicator may show available charge when the battery is close to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 ANA Screen Control Set Recalled by Bio-Rad Laboratories, Inc....
The Issue: A new lot of ANA screen control and any subsequent control lots are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI SHERIDAN SHERI-BRONCH Endobronchial Tube - Product Recalled by...
The Issue: The tracheal and brochial swivel connectors are incorrectly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oral-B Recalled by Young Dental Manufacturing Co, LLC Due to Product shelf...
The Issue: Product shelf life may be shorter than that indicated on the label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XEN Gel Stent Recalled by Allergan PLC Due to Foreign Object Contamination
The Issue: Residual polishing compounds, that are used in the needle sleeve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroDot brand: Wave Prep 4 oz. tubes-Product 1710-03. An electroconductive...
The Issue: Product has the potential to be contaminated with Burkholderia cepacia (B....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroDot brand: Wave Prep Single use cups Recalled by Bio-Signal Group Corp....
The Issue: Product has the potential to be contaminated with Burkholderia cepacia (B....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genius 2 Tympanic Thermometer OEM Tympanic Item Code:303062 Recalled by...
The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genius 2 Tympanic Thermometer Private Label Item Code: 3069 Recalled by...
The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genius 2 Tympanic Thermometer (discontinued) Item Code: 303000 Recalled by...
The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genius 3 Tympanic Thermometer- electric thermometer Item Code: 303013...
The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genius 2 Tympanic Thermometer OEM Tympanic Item Code: 303063 Recalled by...
The Issue: The frequency of calibration for the Genius Tympanic Thermometer as stated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys Anti-HAV IgM assay-for the in vitro qualitative detection of...
The Issue: Current software version of the Anti-HAV IgM APP-file (version 06.05-101)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MAX-CORE Disposable Core Biopsy Instrument - Product Usage: The...
The Issue: During the firm's review of May 2019 complaint data, a significant increase...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal CR Knee Replacement System Model Number: TCR-111-1111-010102 -...
The Issue: Medial and lateral polyethylene inserts did not securely fit into the cobalt...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Python Embolectomy Catheters Recalled by Applied Medical Resources Corp Due...
The Issue: The firm has received reports of tip separation during usage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Applied Medical Dual Lumen Graft Cleaning Catheter & 1cc SYRINGE...
The Issue: The firm has received reports of tip separation during usage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Embolectomy Catheter & 1 ml SYRINGE Recalled by Applied Medical...
The Issue: The firm has received reports of tip separation during usage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.