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. 2,547 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,547 in last 12 months

Showing 2652126540 of 53,528 recalls

FoodJuly 17, 2018· Griffith Labs U.S.A.

Recalled Item: Caesar Seasoning 50 pound bag Item 859086500 Recalled by Griffith Labs...

The Issue: Potential presence of Salmonella due to use of recalled whey ingredient

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 17, 2018· Griffith Labs U.S.A.

Recalled Item: Premix Broccoli Cheddar no Mustard 50 pound bag Recalled by Griffith Labs...

The Issue: Potential presence of Salmonella due to use of recalled whey ingredient

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 17, 2018· Griffith Labs U.S.A.

Recalled Item: Garlic Cheese Crouton Seasoning 50 pound bag Item 859086200 Recalled by...

The Issue: Potential presence of Salmonella due to use of recalled whey ingredient

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 17, 2018· Griffith Labs U.S.A.

Recalled Item: Cold Dough Premix 6.8 pound bag Recalled by Griffith Labs U.S.A. Due to...

The Issue: Potential presence of Salmonella due to use of recalled whey ingredient

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 17, 2018· Griffith Labs U.S.A.

Recalled Item: Deep Pan Pizza Dough 1 pound 4 oz bag Recalled by Griffith Labs U.S.A. Due...

The Issue: Potential presence of Salmonella due to use of recalled whey ingredient

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 17, 2018· Abbott Laboratories, Inc

Recalled Item: Abbott ARCHITECT c16000 Processing Module Recalled by Abbott Laboratories,...

The Issue: There is a potential to generate incorrect results on the instrument if...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Abbott Laboratories, Inc

Recalled Item: Abbott ARCHITECT c4000 Processing Module Recalled by Abbott Laboratories,...

The Issue: There is a potential to generate incorrect results on the instrument if...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Abbott Laboratories, Inc

Recalled Item: Abbott ARCHITECT c8000 Processing Module Recalled by Abbott Laboratories,...

The Issue: There is a potential to generate incorrect results on the instrument if...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Alcon Research Laboratories Ltd.

Recalled Item: Alcon or Endure Ophthalmic Microscope Product Usage: Used for low Recalled...

The Issue: Potential for the optical head to detach from the stand due to the lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 130¿ 11 mm x 440 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 125¿ 13 mm x 440 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 130¿ 11 mm x 320 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 440 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 460 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 130¿ 13 mm x 460 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 125¿ 11 mm x 360 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 130¿ 11 mm x 280 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 130¿ 11 mm x 360 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Right 130¿ 15 mm x 400 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus¿ Hip Fracture Nail Left 130¿ 11 mm x 400 mm Recalled by Zimmer...

The Issue: The set screw is not able to advance or reverse from the original position...

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

Class II — Potential Health HazardOngoing