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.
Showing 31061–31080 of 52,647 recalls
Recalled Item: Nystatin Topical Powder Recalled by X-Gen Pharmaceuticals Inc. Due to...
The Issue: Presence of Foreign Substance: potential presence of plastic particles.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Oral Suspension Recalled by VistaPharm, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Presence of an impurity peak...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QuikClot TraumaPad Recalled by Z-Medica, LLC Due to Packaging breach may...
The Issue: Packaging breach may compromise sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTARAY NAV High-Density Mapping Catheter. Recalled by Biosense Webster,...
The Issue: Contraindication language updated in the Instructions For Use (IFU) to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTARAY NAV High-Density Mapping Catheter. Recalled by Biosense Webster,...
The Issue: Contraindication language updated in the Instructions For Use (IFU) to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventolin HFA (albuterol sulfate) Inhalation Recalled by GlaxoSmithKline, LLC...
The Issue: Defective Delivery System: Elevated number of units with out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mibelas 24 Fe (Norethindrone acetate and Ethinyl estradiol 1 mg/0.02...
The Issue: Contraceptive Tablets Out of Sequence- First 4 pills of the packet are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fish Ball in Polybag 24/12oz. Recalled by Wang Globalnet Due to Undeclared Egg
The Issue: Fish products contain undeclared egg and wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fish Cake in Polybag 20/1lb. Recalled by Wang Globalnet Due to Undeclared Egg
The Issue: Fish products contain undeclared egg and wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fish Cake in Polybag 10/2.2lbs Recalled by Wang Globalnet Due to Undeclared Egg
The Issue: Fish products contain undeclared egg and wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fish Cake in Polybag 10/930g Recalled by Wang Globalnet Due to Undeclared Egg
The Issue: Fish products contain undeclared egg and wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fish Tofu in Polybag 40/240g Recalled by Wang Globalnet Due to Undeclared Egg
The Issue: Fish products contain undeclared egg and wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Multiphor II Electrophoresis System GE HealthCare Product Number: 18-1018-06...
The Issue: Potential for electric shock in the case of a failure to install the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD¿ High Volume Administration Set with FlowStop Recalled by Smiths...
The Issue: One lot of CADD¿ High Volume Administration sets, part number 21-7381-24,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter Synchron AQUA CAL Level 1 Recalled by Beckman Coulter Inc...
The Issue: The firm identified a negative shift of 5mmol/L for sodium recovery in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek LATARJET EXPERIENCE Coracoid Drill Product Code: 288201 Product...
The Issue: Combo Screw Driver (Product Code 288211) tip has the increased potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek LATARJET EXPERIENCE Coracoid Top Hat Drill Product Code:...
The Issue: Combo Screw Driver (Product Code 288211) tip has the increased potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek LATARJET EXPERIENCE Extraction Driver Product Code: 288216...
The Issue: Combo Screw Driver (Product Code 288211) tip has the increased potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek LATARJET EXPERIENCE-Combo Screw Driver Product Code: 288211...
The Issue: Combo Screw Driver (Product Code 288211) tip has the increased potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek LATARJET EXPERIENCE Top Hat Tap Product Code: 288203 Recalled by...
The Issue: Combo Screw Driver (Product Code 288211) tip has the increased potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.