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. 1,057 recalls have been distributed to Massachusetts in the last 12 months.
Showing 18521–18540 of 52,647 recalls
Recalled Item: OSTEORAPTOR CRVD 2.3 SA UB COBRD BLACK- Absorbable Suture anchor Recalled by...
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX ULTRA PLLA/HA 6.5 W/3 UB- Absorbable Suture anchor Product Recalled...
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX AB 5.0 SUTR ANCHR W/2 38 ULTRA-Absorbable Suture anchors Recalled by...
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEALICOIL RSB SA 5.5MM W/1 UT & 1 UB BLK- Recalled by Smith & Nephew, Inc....
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEORAPTOR 2.9 W/ 2 UB WHITE / BLUE -Absorbable Suture Recalled by Smith &...
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX ULTRA 5.5MM PLLA/HA 2 UBWHT/BL--Absorbable Suture anchor Product...
The Issue: Product packaging improper or incomplete seal of the pouch surrounding the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microwave popcorn packaged in the following ways: 1) Full Circle Recalled by...
The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Light microwave popcorn packaged in the following ways: 1) Full Recalled by...
The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lightly salted microwave popcorn packaged in the following ways: 1) Recalled...
The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cadia Organic Unsalted Microwave Popcorn Recalled by Gilster-Mary Lee Corp....
The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Buttered microwave popcorn packaged in the following ways: 1) Full Recalled...
The Issue: Popcorn ingredient was recalled due to foreign matter: tempered glass...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AESCULAP S4 Cervical Cross Connector L 42-58mm Recalled by Aesculap Implant...
The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AESCULAP S4 Cervical Cross Connector L 28-33mm Recalled by Aesculap Implant...
The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AESCULAP S4 Cervical Cross Connector L22mm Recalled by Aesculap Implant...
The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AESCULAP S4 Cervical Cross Connector Recalled by Aesculap Implant Systems...
The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AESCULAP S4 Cervical Cross Connector L24mm Recalled by Aesculap Implant...
The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AESCULAP S4 Cervical Cross Connector L 33-42mm Recalled by Aesculap Implant...
The Issue: Insufficient clamping force of the cross connectors in the spinal surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tomographic Imager Combining Emission Computed Tomography With Nuclear...
The Issue: Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to Potential electrical arc flash...
The Issue: Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to Potential electrical arc flash...
The Issue: Potential electrical arc flash within the Power Gradient & RF (PGR) Cabinet.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.