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. 2,530 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,530 in last 12 months

Showing 3228132300 of 52,647 recalls

Medical DeviceMarch 9, 2017· Smith & Nephew, Inc.

Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...

The Issue: The expiration dates on the labeling are incorrect, the actual expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Smith & Nephew, Inc.

Recalled Item: Peri-Loc(R) VLP 3.5 MM X 6 MM SELF-TAPPING CORTEX SCREW Recalled by Smith &...

The Issue: The expiration dates on the labeling are incorrect, the actual expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Smith & Nephew, Inc.

Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...

The Issue: The expiration dates on the labeling are incorrect, the actual expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Smith & Nephew, Inc.

Recalled Item: D-RAD Recalled by Smith & Nephew, Inc. Due to The expiration dates on the...

The Issue: The expiration dates on the labeling are incorrect, the actual expiration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Cincinnati Sub-Zero Products Inc

Recalled Item: Hemotherm CE Recalled by Cincinnati Sub-Zero Products Inc Due to Improperly...

The Issue: Improperly rated fuses were used in the manufacture of the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Keystone Dental Inc

Recalled Item: Keystone Dental Inc. PrimaConnex Straight Implant TC Recalled by Keystone...

The Issue: Straight PrimaConnex Implants contained Tapered PrimaConnex Implants

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2017· Ion Beam Applications S.A.

Recalled Item: Proteus 235 Recalled by Ion Beam Applications S.A. Due to The Proton Therapy...

The Issue: The Proton Therapy System can allow gantry rotation even if the snout is not...

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

Class II — Potential Health HazardOngoing
DrugMarch 8, 2017· Mckesson Medical Surgical

Recalled Item: hydrALAZINE HYDROCHLORIDE INJECTION Recalled by Mckesson Medical Surgical...

The Issue: Temperature Abuse: Certain pieces of these lots distributed by McKesson...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 8, 2017· Isomeric Pharmacy Solution, LLC

Recalled Item: Triamcinolone 40 mg/mL 2 mL Single-Dose Vial for Injection Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 8, 2017· Gerber Products Company dba Nestle Infant Nutrition

Recalled Item: Gerber¿ Pasta Pick-Ups Cheese Ravioli Net Wt 6 oz (170g) Recalled by Gerber...

The Issue: Gerber Products Company is recalling Cheese Ravioli Gerber¿ Pasta Pick-Ups¿...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 8, 2017· Ortho-Clinical Diagnostics

Recalled Item: enGen (TM) Laboratory Automation Systems using all TCAutomation(TM) Software...

The Issue: Software anomaly; Thermo-Fisher Scientific initially discovered and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2017· Sonesta Medical Ab

Recalled Item: Sonesta S2 Recalled by Sonesta Medical Ab Due to The user / service manual...

The Issue: The user / service manual for the Sonesta S2 Chair contain wrong information...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 03896216 Recalled by Siemens...

The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 02419937 Recalled by Siemens...

The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur BR assay Cat No. 09010686 Recalled by Siemens...

The Issue: Potential for the ADVIA Centaur Syphilis assay to interfere with the BR (CA...

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

Class II — Potential Health HazardOngoing
DrugMarch 7, 2017· Alvogen, Inc

Recalled Item: Nifedipine Extended-Release Tablets Recalled by Alvogen, Inc Due to Cross...

The Issue: Cross Contamination with another product:residual powder found in inlet air...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· Alvogen, Inc

Recalled Item: Nifedipine Extended-Release Tablets Recalled by Alvogen, Inc Due to Cross...

The Issue: Cross Contamination with another product:residual powder found in inlet air...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· Alvogen, Inc

Recalled Item: Adalat CC (nifedipine) Extended Release Tablets 30 mg Recalled by Alvogen,...

The Issue: Cross Contamination with another product:residual powder found in inlet air...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· Alvogen, Inc

Recalled Item: Adalat CC (nifedipine) Extended Release Tablets Recalled by Alvogen, Inc Due...

The Issue: Cross Contamination with another product:residual powder found in inlet air...

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

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2017· Alvogen, Inc

Recalled Item: Nifedipine Extended-Release Tablets Recalled by Alvogen, Inc Due to Cross...

The Issue: Cross Contamination with another product:residual powder found in inlet air...

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

Class III — Low RiskOngoing
Refund