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. 1,077 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
1,077 in last 12 months

Showing 16901–16920 of 52,647 recalls

DrugMarch 31, 2021· QMart

Recalled Item: PremierZen Extreme 3000 Recalled by QMart Due to Marketed without Approved...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2021· QMart

Recalled Item: Burro en Primavera Recalled by QMart Due to Marketed without Approved...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2021· QMart

Recalled Item: Imperial Platinum 2000 Recalled by QMart Due to Marketed without Approved...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2021· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Riomet (metformin hydrochloride oral solution) 500 mg/5 mL Cherry Flavor...

The Issue: Microbial Contamination of Non-Sterile Product

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 31, 2021· Apotex Corp.

Recalled Item: Guanfacine Extended-Release Tablets 2 mg Recalled by Apotex Corp. Due to...

The Issue: Cross Contamination with Other Product: Product is being recalled due to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 31, 2021· Soft Computer Consultants, Inc.

Recalled Item: SoftCytogenetics Recalled by Soft Computer Consultants, Inc. Due to Software...

The Issue: Software is given wrong results going out to HIS on test that had reruns.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: Artis systems - Product Usage: an angiography systems developed for Recalled...

The Issue: Due to inappropriate cleaning, some Artis systems show unexpected corrosion...

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

Class II — Potential Health HazardOngoing
FoodMarch 30, 2021· USA LANKA INC

Recalled Item: Motha Jelly Crystals - Orange Flavoured Jelly Recalled by USA LANKA INC Due...

The Issue: Jelly contains undeclared FD&C Yellow #6

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 30, 2021· USA LANKA INC

Recalled Item: Motha Jelly Crystals - Mango Flavoured Jelly Recalled by USA LANKA INC Due...

The Issue: Jelly contains undeclared FD&C Yellow #5 and FD&C Yellow #6

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 30, 2021· USA LANKA INC

Recalled Item: Motha Jelly Crystals Strawberry Flavoured Jelly Recalled by USA LANKA INC...

The Issue: Jelly contains undeclared FD&C Red #40

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

Class III — Low RiskOngoing
Refund
FoodMarch 30, 2021· USA LANKA INC

Recalled Item: Motha Jelly Crystals - Mixed Fruit Flavoured Jelly Recalled by USA LANKA INC...

The Issue: Jelly contains undeclared FD&C yellow #5 and blue #1, and unapproved...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 30, 2021· USA LANKA INC

Recalled Item: Motha Jelly Crystals - Black Currant Flavoured Jelly Recalled by USA LANKA...

The Issue: Jelly contain undeclared FD&C yellow #5 and blue #1, and unapproved...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 30, 2021· Na Na Collection

Recalled Item: PremierZen Platinum 5000 Recalled by Na Na Collection Due to Marketed...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 30, 2021· Ummzy, LLC

Recalled Item: Krazy Night capsule Recalled by Ummzy, LLC Due to Undeclared Tadalafil

The Issue: Marketed Without An Approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 30, 2021· Ummzy, LLC

Recalled Item: Shogun-X capsules Recalled by Ummzy, LLC Due to Undeclared Tadalafil

The Issue: Marketed Without An Approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 30, 2021· Ummzy, LLC

Recalled Item: Thumbs up 7 Red 70K capsules Recalled by Ummzy, LLC Due to Undeclared Tadalafil

The Issue: Marketed Without An Approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 30, 2021· Na Na Collection

Recalled Item: Triple SupremeZen Gold 3500 Recalled by Na Na Collection Due to Marketed...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 29, 2021· Nuri Trading LLC

Recalled Item: Thumbs Up 7 Black 25K capsule Recalled by Nuri Trading LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: Product found to be tainted with...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 29, 2021· Spartan Chemical Co Inc

Recalled Item: Lite'n Foamy E2 Sanitizing Handwash (Benzalkonium Chloride Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 29, 2021· Spartan Chemical Co Inc

Recalled Item: Lite'n Foamy Healthcare Personnel Handwash (Chloroxylenol Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund