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. 2,542 recalls have been distributed to Massachusetts in the last 12 months.
Showing 23841–23860 of 29,284 recalls
Recalled Item: CelluTome Epidermal Harvesting System Harvester (5.0 CM) STERILE EO Rx...
The Issue: KCI has received reports that, in a small number of cases, the CelluTome...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillators Models: M3535A and M3536A...
The Issue: 1. Device will perform the weekly automated tests hourly, which could cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue TcG10 Recalled by Philips Medical Systems, Inc. Due to...
The Issue: Philips has discovered that the Instructions for Use (IFU) for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Models:M3535A Recalled by...
The Issue: MRx Defib can be susceptible to one or both issues: 1. The C02 Inlet Port...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ECG Out Cable Recalled by Philips Electronics North America Corporation Due...
The Issue: When a Philips monitor/defibrillator is receiving an ECG signal from an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips Medical Systems,...
The Issue: Device may malfunction, which could cause therapy to be delayed, disabled,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System Recalled by Ortho-Clinical Diagnostics...
The Issue: Software Anomaly: the firm has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
The Issue: Software Anomaly: the firm has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Software Anomaly: the firm has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...
The Issue: The cuff inflation line may detach from the endotracheal tube during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...
The Issue: The cuff inflation line may detach from the endotracheal tube during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...
The Issue: The cuff inflation line may detach from the endotracheal tube during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...
The Issue: The cuff inflation line may detach from the endotracheal tube during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Microcuff Subglottic Suctioning Recalled by Halyard Health Due to...
The Issue: The cuff inflation line may detach from the endotracheal tube during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.