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 24681–24700 of 29,284 recalls
Recalled Item: McKesson Medi-Pak Recalled by Medical Action Industries Inc Due to Some of...
The Issue: Some of the sterile kits may have incomplete seals which might compromise...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Max Barrier Kit Recalled by Medical Action Industries Inc Due to Some of the...
The Issue: Some of the sterile kits may have incomplete seals which might compromise...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer EDI PERIARTICULAR PLATING SYSTEM CANCELLOUS BONE SCREW Recalled by...
The Issue: Two lots of screws were commingled. Screws with etching and machining for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laceration/Suture Removal Recalled by Medical Action Industries Inc Due to...
The Issue: Some of the sterile kits may have incomplete seals which might compromise...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EG-3630U Ultrasound Video Gastroscope EG-3830UT Ultrasound Video Gastroscope...
The Issue: Aspiration needles used in combination with Ultrasound Gastroscopes can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tritium Sternal Plate System Recalled by PIONEER SURGICAL TECHNOLOGY, INC....
The Issue: Lack of Sterility Assurance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra¿ LED Battery Charger Recalled by Integra LifeSciences Corp. Due to...
The Issue: LED battery chargers may prematurely fail and will not charge the LED...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DATEX-OHMEDA S/5 SINGLE-WIDTH AIRWAY MODULE Recalled by GE Healthcare, LLC...
The Issue: Failure of the CO2 detector in Single-width Airway and Extension modules,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prosound F75 or F75 The Hitachi Aloka Medical Recalled by Hitachi Aloka...
The Issue: Loosened monitor arm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTAMIX 1200 Compounder Recalled by Baxter Healthcare Corp. Due to If the...
The Issue: If the universal ingredient (UI) in an active configuration is changed using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tenor is a mobile passive lift Recalled by ARJOHUNTLEIGH POLSKA SP. ZO.O....
The Issue: ArjoHuntleigh received reports where the Tenor Lift without Scale (spreader...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coat-A-Count Direct Androstenedione Recalled by Siemens Healthcare...
The Issue: The assay is demonstrating a higher frequency of results greater than 10...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Attest Auto-reader. Model numbers 390 Recalled by 3M Company - Health...
The Issue: Labeling on units shipped prior to May 16th, 2014 did not contain the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MC-500 Multicolor Laser Photocoagulator Recalled by Nidek Inc Due to Laser...
The Issue: Laser aperture label was not affixed to device prior to shipment in the US.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Medical System Allura Xper X-Ray Angiographic Recalled by Philips...
The Issue: In certain circumstances, a software error can lead to a situation where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Hospira MedNet Medication Management Suite (MMS). Product Usage: The...
The Issue: Hospira MedNet 5.5, 5.8.1, and 5.8.2 contains software defect where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Healthcare Qube Compact Monitor Recalled by Spacelabs Healthcare...
The Issue: Spacelabs Healthcare is recalling Qube Compact Monitor, Model 91390, due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrypticaseTM Soy Agar with 5% Sheep Blood (TSA IITM) // Recalled by Becton...
The Issue: A low level of surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACS Canto and associated Fluidics Cart Product Usage: Flow Recalled by...
The Issue: Laser cooling fans and internal fan of the associated fluidics cart are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDC Anaerobe 5% Sheep Blood Agar CDC Anaerobe 5% Sheep Recalled by Becton...
The Issue: A low level of surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.