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. 2,493 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,493 in last 12 months

Showing 3960139620 of 52,647 recalls

Medical DeviceJuly 2, 2015· Silhouette Lift, Inc.

Recalled Item: Silhouette Lift brochure Silhouette Sutures are for use in midface Recalled...

The Issue: Silhouette Lift is recalling the Silhouette Suture brochure because it does...

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

Class II — Potential Health HazardOngoing
FoodJuly 2, 2015· Barilla America NY, Inc.

Recalled Item: Barilla Pronto PENNE Recalled by Barilla America NY, Inc. Due to Barilla...

The Issue: Barilla America NY, Inc. has recalled four types of pasta due to the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 2, 2015· Barilla America NY, Inc.

Recalled Item: Barilla Packaged Specifically for FoodService Recalled by Barilla America...

The Issue: Barilla America NY, Inc. has recalled four types of pasta due to the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 2, 2015· Arthur Schuman Inc.

Recalled Item: Bella Rosa Parmesan Net Wt. 20 oz (567 g) 1.25 LB Arthur Schuman Recalled by...

The Issue: Bella Rosa Grated Parmesan Cheese may contain undeclared egg lysozyme.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJuly 2, 2015· Barilla America NY, Inc.

Recalled Item: Barilla PENNE Recalled by Barilla America NY, Inc. Due to Barilla America...

The Issue: Barilla America NY, Inc. has recalled four types of pasta due to the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 2, 2015· Barilla America NY, Inc.

Recalled Item: Barilla MEDIUM SHELLS Recalled by Barilla America NY, Inc. Due to Barilla...

The Issue: Barilla America NY, Inc. has recalled four types of pasta due to the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2015· Bestco, Inc.

Recalled Item: CVS SUGAR FREE BLACK CHERRY COUGH DROPS (MENTHOL-COUGH SUPPRESSANT) Recalled...

The Issue: Presence of Foreign Tablets/Capsules: Presence of comingled Sugar Free Honey...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJuly 2, 2015· XTREME Z DISTRIBUTORS INC

Recalled Item: Zero Xtreme High Performance Fat Burner capsules Recalled by XTREME Z...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling and analysis confirmed...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF Base CT/PET System. The Philips GEMINI PET/CT Imaging Recalled by...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI LXL CT/PET System. The Philips GEMINI PET/CT Imaging Systems Recalled...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Myoscience Inc

Recalled Item: iovera 155 Smart Tip Recalled by Myoscience Inc Due to The expiration date...

The Issue: The expiration date on the outer box label and the pouch label for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF Ready CT/PET System. The Philips GEMINI PET/CT Imaging Recalled by...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF 64 Slice CT/PET System. The Philips GEMINI PET/CT Recalled by...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF Big Bore CT/PET System. The Philips GEMINI PET/CT Recalled by...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF 16 Slice CT/PET System. The Philips GEMINI PET/CT Recalled by...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI GXL 16 Slice CT/PET System. The Philips GEMINI PET/CT Recalled by...

The Issue: Philips has identified four (4) software defects in the Tumor LOC software...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software anomaly may...

The Issue: Software anomaly may occur during the installation of an Assay Data Diskette...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Remel Inc

Recalled Item: PathoDx Strep Grouping Kit Recalled by Remel Inc Due to A reagent present...

The Issue: A reagent present may produce weak or slow reactions; continued use may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· BIOTRONIK, Inc.

Recalled Item: PSW 1203.U/1 Recalled by BIOTRONIK, Inc. Due to Ventricular packing: LV...

The Issue: Ventricular packing: LV software programming versions for BIOTRONIK CRT-P...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/ zeego systems Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: in case a system error occurs and the system enters the "Bypass Fluoro" mode...

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

Class II — Potential Health HazardOngoing