Product Recalls in Delaware

Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,830 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
1,830 in last 12 months

Showing 2006120080 of 48,330 recalls

Medical DeviceOctober 24, 2019· Boston Scientific Corporation

Recalled Item: NC Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene...

The Issue: Certain dilation and extension catheters are being recalled because these...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Boston Scientific Corporation

Recalled Item: Guidezilla II Guide Extension Catheter Sterilized using ethylene oxide....

The Issue: Certain dilation and extension catheters are being recalled because these...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Boston Scientific Corporation

Recalled Item: Rebel Monorail PtCr Coronary Stent System Recalled by Boston Scientific...

The Issue: Certain dilation and extension catheters are being recalled because these...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Boston Scientific Corporation

Recalled Item: Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene oxide....

The Issue: Certain dilation and extension catheters are being recalled because these...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion Medical Products UNIVERSAL LINE FULL BODY DRAPE KIT - Recalled by...

The Issue: Sterile packaging incomplete seals may compromise sterility of the product

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

Class II — Potential Health HazardOngoing
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Regular Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Regular Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Regular Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Regular Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund