Product Recalls in Indiana

Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,535 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,535 in last 12 months

Showing 3250132520 of 53,528 recalls

DrugFebruary 10, 2017· Synergy Rx

Recalled Item: CLOBETASOL 0.05% IN OLEA BASE Recalled by Synergy Rx Due to Lack of...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: HYDROCORTISONE 2.5% WITH ALOE VERA CREAM Recalled by Synergy Rx Due to Lack...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: TRI-BLEACHING CREAM (Retinoic Acid 0.1% Recalled by Synergy Rx Due to Lack...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: CUSTOM LIGHTENING/BRIGHTENING CREAM Recalled by Synergy Rx Due to Lack of...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: LP CREAM (Lidocaine 15%/Prilocaine 5%) Recalled by Synergy Rx Due to Lack of...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: REVERSE DML LOTION (Ketoconazole 2% Recalled by Synergy Rx Due to Lack of...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Hospira Inc., A Pfizer Company

Recalled Item: METRONIDazole Injection Recalled by Hospira Inc., A Pfizer Company Due to...

The Issue: Lack of Sterility Assurance: customer report of leaking bag

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: PURIFIED WATER Recalled by Synergy Rx Due to Lack of Assurance of Sterility:...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: DICLOFENAC 3% and 5% LIP BALM and DICLOFENAC 5% SPF 30 LIP BALM Recalled by...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: TACROLIMUS 0.1% Ointment and TACROLIMUS 0.1%/KETOCONAZOLE 2% Recalled by...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: UREA 40% Cream Recalled by Synergy Rx Due to Lack of Assurance of Sterility:...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: LTP (Lidocaine 10% Recalled by Synergy Rx Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2017· Synergy Rx

Recalled Item: DUO Cream (Retinoic Acid 0.05% Recalled by Synergy Rx Due to Lack of...

The Issue: Lack of Assurance of Sterility: There are also CGMP Deviations.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 9, 2017· Remel Inc

Recalled Item: Remel Recalled by Remel Inc Due to Test organisms exhibit poor growth when...

The Issue: Test organisms exhibit poor growth when grown using the test agar. The poor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2017· Cardiovascular Systems Inc

Recalled Item: ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire Recalled by...

The Issue: CSI is recalling three lots of VIPERWIRE ADVANCE WITH FLEXTIP PERIPHERAL...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2017· Medtronic

Recalled Item: BNX Fine Need Aspiration System (22GA) Recalled by Medtronic Due to Handle...

The Issue: Handle may break during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2017· Medtronic

Recalled Item: BNX Fine Need Aspiration System (19GA) Recalled by Medtronic Due to Handle...

The Issue: Handle may break during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2017· Medtronic

Recalled Item: SharkCore Fine Needle Biopsy System (25GA) Recalled by Medtronic Due to...

The Issue: Handle may break during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2017· Medtronic

Recalled Item: SharkCore LG Fine Needle Biopsy System (19GA) Recalled by Medtronic Due to...

The Issue: Handle may break during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2017· Medtronic

Recalled Item: SharkCore Fine Needle Biopsy System (22 GA) Recalled by Medtronic Due to...

The Issue: Handle may break during use.

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

Class II — Potential Health HazardOngoing