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. 2,618 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,618 in last 12 months

Showing 1718117200 of 29,284 recalls

Medical DeviceDecember 4, 2017· Konica Minolta Medical Imaging USA, Inc.

Recalled Item: Sonimage HS1 Ultrasound Kit AC adapter Recalled by Konica Minolta Medical...

The Issue: There is a risk of circuit board breakage within the main housing of the AC...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2017· Fresenius Vial Sa

Recalled Item: Volumat MC Agilia Volumetric Infusion Pump Recalled by Fresenius Vial Sa Due...

The Issue: Fresenius Kabi initiated a mandatory software upgrade of the Volumat MC...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2017· ProSun International, LLC

Recalled Item: Sundream 12 V tanning bed Recalled by ProSun International, LLC Due to The...

The Issue: The 30 minute maximum tanning time has been reduced to 20 minutes.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2017· Mako Surgical Corporation

Recalled Item: RESTORIS MCK TIBIAL BASEPLATE-RM/LL used in unicompartmental knee...

The Issue: Incorrect product and/or label. Sizing is labeled incorrectly.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2017· Elekta, Inc.

Recalled Item: ELEKTA Digital Accelerator under the following brand names: Elekta Synergy...

The Issue: There is a potential for an uncontrolled extension of iViewGT / XVI detector...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2017· Ohmeda Medical

Recalled Item: Rotating IV Pole Rotating IV Pole falls under the category Recalled by...

The Issue: There is the potential for the Rotating IV Pole to fall. A fall could result...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2017· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Gas Module 3 monitoring spirometer Recalled by Mindray DS USA, Inc. dba...

The Issue: The firm made multiple changes to the product requiring the submission of a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: VERSYS 10 INCH BEADED FC REV 13.5X250MM BWD LT and Recalled by Zimmer...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: Persona Partial Knee spacer block instruments Recalled by Zimmer Biomet,...

The Issue: Certain partial knee implant spacer blocks do not fit in the alignment tower...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Dental Inc

Recalled Item: Tapered Screw-Vent MTX Recalled by Zimmer Dental Inc Due to Mislabeling

The Issue: Two lots of the Tapered Screw-Vent Implants, with different outer thread...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Dental Inc

Recalled Item: Tapered Screw-Vent MTX Recalled by Zimmer Dental Inc Due to Mislabeling

The Issue: Two lots of the Tapered Screw-Vent Implants, with different outer thread...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: NP FEM LT SZ0 NATURAL-KNE NP FEM RT SZ0 NATURAL-KNE Recalled by Zimmer...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: PRCT MIS CR MOB PLT SZ 4 L¿ PRCT MIS Recalled by Zimmer Biomet, Inc. Due to...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: VERSYS 10 INCH BEADED FC REV 15.0X250MM BWD LT & Recalled by Zimmer Biomet,...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: CR-FLEX OPT FEM C-R MINUS CR-FLEX OPT FEM D-L MINUS Recalled by Zimmer...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: NEXGEN GSF POROUS FEMORAL LPS FLEX SIZE F Recalled by Zimmer Biomet, Inc....

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: LPS PRECOAT SRF HDN FEM SZ D-L LPS PRECOAT SRF Recalled by Zimmer Biomet,...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: ZIMMER PATELLA FEMORAL JOINT¿ Osteoarthritis Recalled by Zimmer Biomet, Inc....

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: NEXGEN LPS-FLEX PRECOAT FEMORAL SIZE E-LT This device is indicated Recalled...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2017· Zimmer Biomet, Inc.

Recalled Item: VERSYS 7.5 INCH BEADED FC REV 13.5X190MM STRAIGHT Prosthesis Recalled by...

The Issue: The LDPE bag packaging for various highly polished hip and knee implants may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing