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. 2,456 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,456 in last 12 months

Showing 4518145200 of 53,528 recalls

DrugApril 14, 2014· P&L Developments, LLC

Recalled Item: Day Time Cold & Flu Recalled by P&L Developments, LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: Phenylephrine component is subpotent.

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

Class III — Low RiskOngoing
Refund
DrugApril 14, 2014· Golden State Medical Supply Inc.

Recalled Item: LOSARTAN POTASSIUM Tablets Recalled by Golden State Medical Supply Inc. Due...

The Issue: Presence of Foreign Substance; some bottles may contain debris that was...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 14, 2014· Arrow International Inc

Recalled Item: Arrow¿ Percutaneous Sheath Introducer Kits The Percutaneous sheath...

The Issue: Arrow is recalling the Arrow¿ Percutaneous Sheath Introducer Kits due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Merit Medical Systems, Inc.

Recalled Item: Merit Laureate Hydrophilic Guide Wire Recalled by Merit Medical Systems,...

The Issue: Discrepancy between the carton and unit labeling for the Merit Laureate...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Tenex Health Inc

Recalled Item: TX1 Tissue Removal System. TX1 Procedure Pack P/N 554-1003-001 (outer box)...

The Issue: The sterile barrier in the packaging may be compromised due to cracks in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Compact Plus Test Strips For use with: ACCU-CHEK Compact Plus...

The Issue: Roche Diabetes Care has become aware the ACCU-CHEK Compact Plus test strips...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Merit Medical Systems, Inc.

Recalled Item: Merit Laureate 0.035" (0.89mm) Hydrophilic Guide Wire Recalled by Merit...

The Issue: Merit Medical Systems, Inc. is voluntarily conducting a recall due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Disposable Centrifugal Pump with X-Coating Recalled by Terumo...

The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Cardiovascular Procedure Kit containing Disposable Centrifugal Pumphead with...

The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Disposable Centrifugal Pump without X-Coating Recalled by Terumo...

The Issue: During set-up and priming of the bypass circuit, leaks were detected on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2014· Ivoclar Vivadent, Inc.

Recalled Item: bluephase style Light probe Pin-point 6>2 mm black REF # Recalled by Ivoclar...

The Issue: A stock check revealed broken glass fibers between the connector and the...

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

Class II — Potential Health HazardOngoing
FoodApril 14, 2014· Health Matters America Inc.

Recalled Item: Organic traditions DARK CHOCOLATE SACHA INCHI SEEDS***DAIRY & SUGAR FREE...

The Issue: Undeclared milk allergen

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 14, 2014· Health Matters America Inc.

Recalled Item: Organic traditions DARK CHOCOLATE GOLDEN BERRIES***DAIRY & SUGAR FREE 80%...

The Issue: Undeclared milk allergen

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 14, 2014· Orange Peel Enterprises, Inc.

Recalled Item: Greens+ Vegan Crisp Bars - Dark Chocolate Almond Coffee Crisp Recalled by...

The Issue: Undeclared milk protein in chocolate coating.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodApril 14, 2014· Orange Peel Enterprises, Inc.

Recalled Item: Greens+ Vegan Crisp Bars - Dark Chocolate Almond Blueberry in 1.4 oz...

The Issue: Undeclared milk protein in chocolate coating.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodApril 14, 2014· Orange Peel Enterprises, Inc.

Recalled Item: Greens+ Vegan Crisp Bars - Dark Chocolate Peanut Butter in 1.4 oz packages....

The Issue: Undeclared milk protein in chocolate coating.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodApril 11, 2014· Kroger Co

Recalled Item: PRIVATE SELECTION SWEET STRAWBERRY SORBET Recalled by Kroger Co Due to...

The Issue: The firm was notified of the presence of undeclared milk in the product.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 11, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Luminos dRFsystem The Axiom Luminos dRF is intended to Recalled by...

The Issue: It was determined that under rare environmental conditions (i.e., extremely...

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

Class II — Potential Health HazardOngoing
FoodApril 11, 2014· Strong America Limited

Recalled Item: GOLDEN SMELL brand Hot Pot Meat Ball Medly Recalled by Strong America...

The Issue: The product was found to contain undeclared eggs based on sampling and...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugApril 11, 2014· Aaron Industries Inc

Recalled Item: Maximum Strength/Non-Drowsy Tussin DM Adult Maximum Strength Recalled by...

The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...

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

Class III — Low RiskOngoing
Refund