Product Recalls in Massachusetts
Product recalls affecting Massachusetts — including food, drugs, consumer products, medical devices, and vehicles distributed to Massachusetts. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,710 recalls have been distributed to Massachusetts in the last 12 months.
Showing 8221–8240 of 29,284 recalls
Recalled Item: BD Connecta" Plus3 White Blend OEM (sterile Recalled by Becton Dickinson &...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Connecta Stopcock Without Extension Tube Catalog No. 394605 (OUS)...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Connecta 3-Way Stopcocks Catalog No. 394900 (OUS) Recalled by Becton...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Connecta Stopcock with OFF Directed Tap Without Extension Tube Recalled...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VOLISTA StandOP Surgical Light Recalled by Getinge Usa Sales Inc Due to...
The Issue: Paint particles may detach and fall in the operating field. In the worst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STIK" plus: Clostridium perfringens Recalled by Microbiologics Inc Due...
The Issue: Labeling error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Three-Lumen CVC Recalled by ARROW INTERNATIONAL Inc. Due to Gravity...
The Issue: Gravity flow rates on the affected product lidstock are incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Battery Recalled by Medtronic Inc Due to Batteries for the HVAD...
The Issue: Batteries for the HVAD system have a weld defect affecting internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nester Embolization Microcoil RPN GPN MWCE-18-5-2-NESTER G52733...
The Issue: The loading cartridges included with these devices may contain a small,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tornado Embolization Microcoil Recalled by Cook Incorporated Due to The...
The Issue: The loading cartridges included with these devices may contain a small,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hilal Embolization Microcoil Recalled by Cook Incorporated Due to The...
The Issue: The loading cartridges included with these devices may contain a small,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DJO EMPOWR 3D Knee (Right) 10mm Tibial Insert Recalled by Encore Medical, LP...
The Issue: A right, size 8, knee tibial insert package may include a mispackaged, left...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux 200NRe Dialyzer Finished Assy. Recalled by Fresenius Medical Care...
The Issue: Dialyzers were distributed after being exposed to cold temperatures which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK Recalled by...
The Issue: One manufacturing lot is missing the plasma-spray coating in the proximal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: illumina Model NextSeq 550 Dx Recalled by Illumina, Inc. Due to...
The Issue: cybersecurity vulnerability
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: illumina Model: MiSeq Dx illumina Model: Recalled by Illumina, Inc. Due to...
The Issue: cybersecurity vulnerability
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STORZ KARL STORZ-ENDOSKOPE CMOS Video Cysto-Urethroscope Recalled by Karl...
The Issue: The endoscope may experience a loss of image when activating monopolar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM Vital Patient Interface 4.0 (P/N: NIM4CPB1) NIM with Software version...
The Issue: Software anomaly was identified.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ratcheting Screwdriver Handle Recalled by Tornier, Inc Due to The device is...
The Issue: The device is unable to meet sterilization requirements when sterilized per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM Vital Console 4.0 (P/N: NIM4CM01) NIM with Software version 1.3.2...
The Issue: Software anomaly was identified.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.