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. 2,574 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,574 in last 12 months

Showing 2082120840 of 29,284 recalls

Medical DeviceApril 15, 2016· Merge Healthcare, Inc.

Recalled Item: Merge LIS software. The firm name on the label is Recalled by Merge...

The Issue: There are potential issues with results reporting for certain run-based...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to Potential...

The Issue: Potential non-recoverable loss of image acquisition. The affected Discovery...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to Potential...

The Issue: Potential non-recoverable loss of image acquisition. The affected Discovery...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Carestream Health Inc

Recalled Item: CARESTREAM Image Suite V4 Recalled by Carestream Health Inc Due to...

The Issue: Carestream Health received a complaint related to CARESTREAM Image Suite 4...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Zimmer Trabecular Metal Technology, Inc.

Recalled Item: TM CR TIB SZ 3 C-H Recalled by Zimmer Trabecular Metal Technology, Inc. Due...

The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Biomerieux France Chemin De L'Or

Recalled Item: VIDAS NT-pro-BNP Product Usage: VIDAS¿ NTproBNP (PBNP) is an automated...

The Issue: Due to a packaging error; The kit does not contain the correct number of C1...

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

Class III — Low RiskOngoing
Medical DeviceApril 15, 2016· Carestream Health Inc

Recalled Item: CARESTREAM Image Suite V3: MINI-PACS/F IMG ST/CLASSIC: REF/Catalog # 1036490...

The Issue: Carestream Health received a complaint related to CARESTREAM Image Suite 4...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Zimmer Trabecular Metal Technology, Inc.

Recalled Item: 00720504022 ACETAB.CUPW/SH Recalled by Zimmer Trabecular Metal Technology,...

The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Zimmer Trabecular Metal Technology, Inc.

Recalled Item: POROUS PATELLA 32MM X 10MM - 00587806532 POROUS PATELLA 35MM Recalled by...

The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Zimmer Trabecular Metal Technology, Inc.

Recalled Item: REV. SHELL LINER 0D 28X48 00700504828 REV. SHELL LINER 10D Recalled by...

The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2016· Toshiba American Medical Systems Inc

Recalled Item: MEXL-3010/A5- Vantage Titan 3T Magnetic Resonance Imaging System Product...

The Issue: A potential problem associated to the gradient coil (ASGC) in the Titan 3T...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2016· Biosense Webster, Inc.

Recalled Item: Pentaray NAV High-Density Mapping Catheter Recalled by Biosense Webster,...

The Issue: Biosense Webster is recalling the Pentaray Catheters to clarify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2016· B. Braun Medical, Inc.

Recalled Item: Non-Vented Dispensing Pin with One-Way Valve and Luer Lock Ultrasite...

The Issue: BBMI recently identified a potential for a tear in the outer blister...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2016· B. Braun Medical, Inc.

Recalled Item: Non-Vented Dispensing Pin with Luer Lock Ultrasite Valve Product Usage:...

The Issue: BBMI recently identified a potential for a tear in the outer blister...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo Dynamics Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...

The Issue: Siemens has identified changes in default carry forward workflow using...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2016· Affymetrix Inc

Recalled Item: CytoScan¿ Dx Assay. The CytoScan Dx Assay consists of five reagent modules...

The Issue: During a recent Ohio site inspection by the FDA it was discovered that...

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

Class III — Low RiskOngoing
Medical DeviceApril 14, 2016· Biosense Webster, Inc.

Recalled Item: Pentaray NAV High-Density Mapping ECO Catheter Recalled by Biosense Webster,...

The Issue: Biosense Webster is recalling the Pentaray Catheters to clarify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2016· Randox Laboratories, Limited

Recalled Item: Magnesium on RX Imola analyser IVD Recalled by Randox Laboratories, Limited...

The Issue: According to the firm, Carry over was observed when the amylase or...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2016· Beckman Coulter Inc.

Recalled Item: Cholesterol Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...

The Issue: Beckman Coulter has identified that Dipyrone (Metamizole) may cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2016· Medtronic

Recalled Item: Battery Pack Used with the Capnostream"20 and Capnostream"20p Patient...

The Issue: Medtronic Respiratory & Monitoring Solutions Announces a Voluntary Recall of...

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

Class I — Serious Health HazardOngoing