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.
Showing 21121–21140 of 52,647 recalls
Recalled Item: TandemLife ECLS Procedure Kit - V24/A17 Recalled by Cardiac Assist, Inc Due...
The Issue: The kit contained a 29Fr ProtekDuo cannula instead of a 24Fr Protek Solo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OARTRAC PROSTATE IMMOBILIZATION ENDORECTAL BALLOON DEVICE KIT Recalled by...
The Issue: May result in readings outside of the expected accuracy range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OARtrac PLUS CLINICAL DETECTOR UNIT Catalog Number: OTS-V2-Plus - Product...
The Issue: May result in readings outside of the expected accuracy range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-PSD HDR Recalled by Angiodynamics, Inc. Due to May result in readings...
The Issue: May result in readings outside of the expected accuracy range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-PSD Electron Recalled by Angiodynamics, Inc. Due to May result in...
The Issue: May result in readings outside of the expected accuracy range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-PSD EXTERNAL BEAM PHOTON Recalled by Angiodynamics, Inc. Due to May...
The Issue: May result in readings outside of the expected accuracy range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViewRay System: Model No. 10000 and 20000 for radiation treatment. Recalled...
The Issue: Registering dose and structures in the treatment delivery workflow could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Paltop Dynamic Dental Implant Dia 3.25mm L 13.0 mm Recalled by Paltop...
The Issue: Some of the implants were packaged with a Standard Platform Cover Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation stand-alone software treatment planning system Recalled by...
The Issue: Editing a static arc beam may unexpectedly set the MU of the beam to its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA SYSTEM CONROL N + P (ref. 00678) Recalled by Diagnostica Stago, Inc. Due...
The Issue: A positive bias was confirmed to exists on the STA - Unicalibrator levels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA UNICALIBRATOR (ref. 00675) Recalled by Diagnostica Stago, Inc. Due to A...
The Issue: A positive bias was confirmed to exists on the STA - Unicalibrator levels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOND Polymer Detection Kit Recalled by Leica Microsystems, Inc. Due to BOND...
The Issue: BOND Polymer Detection kits (DS9800) were held out of storage longer than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Habib EUS RFA Recalled by Boston Scientific Corporation Due to During...
The Issue: During testing on the Habib EUS RFA device, a temperature increase was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Habib EUS RFA Recalled by Boston Scientific Corporation Due to During...
The Issue: During testing on the Habib EUS RFA device, a temperature increase was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Timolol Maleate USP Recalled by Rising Pharmaceuticals, Inc. Due to...
The Issue: Labeling: Label mix-up: A case of Timolol Maleate Sterile Ophthalmic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol Maleate Sterile Opthalmic Solution Recalled by Rising...
The Issue: Labeling: Label mix-up: A case of Timolol Maleate Sterile Ophthalmic...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colostat Recalled by Grato Holdings, Inc. Due to Labeling mix-up -...
The Issue: Labeling mix-up - Indications on product label are incorrect.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MYORISAN (isotretinoin capsules Recalled by Akorn, Inc. Due to Unit Dose...
The Issue: Unit Dose Mispackaging: Customer complaint that a carton labeled as Myorisan...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobetasol Propionate Foam Recalled by Glenmark Pharmaceuticals Inc., USA...
The Issue: Defective delivery system; product is not foaming or is coming out as liquid.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobetasol Propionate Foam (Emulsion Formulation) Recalled by Glenmark...
The Issue: Defective delivery system; product is not foaming or is coming out as liquid.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.