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 16941–16960 of 52,647 recalls

Medical DeviceMarch 26, 2021· Radiometer Medical ApS

Recalled Item: PIC070 Arterial Blood Sampler PICO70 - Product Usage: Preheparinized...

The Issue: Radiometer has become aware of an issue with PICO70 Arterial Blood Sampler....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2021· Ortho-Clinical Diagnostics, INc.

Recalled Item: VITROS¿ Black Slides CATALOG #: J02316 - Product Usage: Recalled by...

The Issue: Delayed results. Ortho confirmed that two lots of VITROS Black Slides are...

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

Class II — Potential Health HazardOngoing
DrugMarch 26, 2021· Antoto-K

Recalled Item: Thumbs Up 7 Red 70K Recalled by Antoto-K 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 26, 2021· Lupin Pharmaceuticals Inc.

Recalled Item: Cefprozil for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...

The Issue: Superpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2021· S & B Story LLC

Recalled Item: Imperial Extreme 2000 Capsules Recalled by S & B Story LLC 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 25, 2021· Namoo Enterprise LLC

Recalled Item: PremierZen Black 5000 capsules Recalled by Namoo Enterprise LLC Due to...

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 25, 2021· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Metformin HCl Extended-Release Tablets Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Moisture Limits: Out of specification for water content

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

Class III — Low RiskOngoing
Refund
DrugMarch 25, 2021· Cosette Pharmaceuticals, Inc.

Recalled Item: Mometasone Furoate Topical Solution Recalled by Cosette Pharmaceuticals,...

The Issue: CGMP Deviaitons

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: 10 G Coxaxial Cannula with Tuohy Connection Recalled by Zavation Due to...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty System Recalled by Zavation Due to Products distributed as sterile...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: 11G DIAMOND TROCAR/CANNULA. For use in Orthopedic / spinal procedures....

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty Direct Bipedicular Bone Access Kit with Drill Recalled by Zavation...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: 10G DOUBLE CEMENT DELIVERY KIT (8 FILLERS). For use in Recalled by Zavation...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty Bipedicular Cement Delivery Cannula Recalled by Zavation Due to...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: InterV Recalled by Zavation Due to Products distributed as sterile may not...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty Recalled by Zavation Due to Products distributed as sterile may not...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: InterV CurvePlus Kit Recalled by Zavation Due to Products distributed as...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: 11G BEVELED TROCAR/CANNULA. For use in Orthopedic / spinal procedures....

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty Direct Access Beveled Tip Trocar Recalled by Zavation Due to...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2021· Zavation

Recalled Item: ZVplasty Drill Recalled by Zavation Due to Products distributed as sterile...

The Issue: Products distributed as sterile may not have been adequately sterilized

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

Class II — Potential Health HazardOngoing