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. 963 recalls have been distributed to Massachusetts in the last 12 months.
Showing 45181–45200 of 52,647 recalls
Recalled Item: Pleo Quent CAPSULES 4X Recalled by Terra-Medica Inc. Due to Penicillin Cross...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pleo Not PORTABLE SIPS 7X Recalled by Terra-Medica Inc. Due to Penicillin...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pleo Ex PORTABLE SIPS 5X Recalled by Terra-Medica Inc. Due to Penicillin...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pleo Not TABLETS 5X Recalled by Terra-Medica Inc. Due to Penicillin Cross...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pleo-Fort DROPS 5X Recalled by Terra-Medica Inc. Due to Penicillin Cross...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pleo Quent SUPPOSITORIES 3X Recalled by Terra-Medica Inc. Due to Penicillin...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pleo Not SUPPOSITORIES 3X Recalled by Terra-Medica Inc. Due to Penicillin...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ritalin HCl (methylphenidate HCl) USP Recalled by Novartis Pharmaceuticals...
The Issue: Labeling: Incorrect or Missing Package Insert; The back of the Medication...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ritalin HCl (methylphenidate HCl) USP Recalled by Novartis Pharmaceuticals...
The Issue: Labeling: Incorrect or Missing Package Insert; The back of the Medication...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pleo Nota- Quent DROPS 5X Recalled by Terra-Medica Inc. Due to Penicillin...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pleo Ex SUPPOSITORIES 3X Recalled by Terra-Medica Inc. Due to Penicillin...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pleo Ex DROPS 5X Recalled by Terra-Medica Inc. Due to Penicillin Cross...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pleo Fort CAPSULES 4X Recalled by Terra-Medica Inc. Due to Penicillin Cross...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pleo Not PORTABLE SIPS Recalled by Terra-Medica Inc. Due to Penicillin Cross...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pleo Quent DROPS 5X Recalled by Terra-Medica Inc. Due to Penicillin Cross...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morph AccessPro Steerable Introducer Recalled by Biocardia, Inc. Due to Firm...
The Issue: Firm discovered the potential for particulates in the inner lumen of Morph...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FIBERNET Embolic Protection System: Recommended Vessel Diameter 3.5 0 5.0 mm...
The Issue: Medtronic is recalling a specific subset of lot numbers of the FIBERNET...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Morph AccessPro Steerable Introducer Recalled by Biocardia, Inc. Due to Firm...
The Issue: Firm discovered the potential for particulates in the inner lumen of Morph...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FIBERNET Embolic Protection System: Recommended Vessel Diameter 5.0 -6.0 mm...
The Issue: Medtronic is recalling a specific subset of lot numbers of the FIBERNET...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FIBERNET Embolic Protection System: Recommended Vessel Diameter 6.0 -7.0 mm...
The Issue: Medtronic is recalling a specific subset of lot numbers of the FIBERNET...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.