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. 2,526 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,526 in last 12 months

Showing 3426134280 of 53,528 recalls

FoodAugust 30, 2016· BIMBO Bakeries USA Inc.

Recalled Item: Entenmann's Little Bites Fudge Brownies - 20 muffins Recalled by BIMBO...

The Issue: Presence of plastic in muffins and brownies.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 30, 2016· BIMBO Bakeries USA Inc.

Recalled Item: Entenmann's Little Bites Variety - 20 pouches labeled for resale Recalled by...

The Issue: Presence of plastic in muffins and brownies.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 30, 2016· Snyder's-Lance Inc.

Recalled Item: Diamond of California¿ Chopped Macadamia Nuts 4oz Recalled by Snyder's-Lance...

The Issue: Product may be potentially contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 30, 2016· BIMBO Bakeries USA Inc.

Recalled Item: Entenmann's Little Bites Chocolate Chip Muffins Recalled by BIMBO Bakeries...

The Issue: Presence of plastic in muffins and brownies.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 30, 2016· Snyder's-Lance Inc.

Recalled Item: Diamond of California¿ Macadamia Halves and Pieces 2.25oz packages Recalled...

The Issue: Product may be potentially contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 30, 2016· Actavis Laboratories, FL, Inc.

Recalled Item: Ramipril Capsules Recalled by Actavis Laboratories, FL, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Lot And/or Exp Date: Bottles labeled with the...

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

Class III — Low RiskOngoing
Refund
DrugAugust 29, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: ZENATANE (isotretinoin capsules USP) 20 mg Recalled by Dr. Reddy's...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 29, 2016· ConMed Corporation

Recalled Item: CONCEPT HEATWAVE Electrode 130 mm x 2.3 mm diameter Recalled by ConMed...

The Issue: CONMED received complaints of damage to the CS-023 electrodes shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: BioFlo PICC with ENDEXO and PASV Valve Technology Maximal Barrier Recalled...

The Issue: Medline Industries, Inc. supplies Navilyst with sterile package gloves...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: LFIT Anatomic V40 Femoral Head Recalled by Stryker Howmedica Osteonics Corp....

The Issue: Stryker received several complaints describing incidence of harm secondary...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· Smith & Nephew, Inc.

Recalled Item: TANDEM (TM) COCR SHELL UHMWPE LINER BIPOLAR Recalled by Smith & Nephew, Inc....

The Issue: Some Bipolar shells were manufactured with an out of specification retainer...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· Trimed Inc

Recalled Item: TriMed Semi-Tubular Plate Recalled by Trimed Inc Due to TriMed is recalling...

The Issue: TriMed is recalling the Semi-Tubular Plates with 10 holes (SMTP-10) because...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: BioFlo PICC with ENDEXO Technology Maximal Barrier Nursing Kit - Recalled by...

The Issue: Medline Industries, Inc. supplies Navilyst with sterile package gloves...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· Smith & Nephew, Inc.

Recalled Item: TANDEM (TM) INTL COCR SHELL UHMWPE LINER BIPOLAR Recalled by Smith & Nephew,...

The Issue: Some Bipolar shells were manufactured with an out of specification retainer...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Xcela Power Injectable PICC Maximal Barrier Nursing Kit The Maximal Recalled...

The Issue: Medline Industries, Inc. supplies Navilyst with sterile package gloves...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2016· Abbott Medical Optics Inc. (AMO)

Recalled Item: TECNIS OptiBlue 1-Piece Intraocular Lens (IOL) Recalled by Abbott Medical...

The Issue: Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2016· Abbott Medical Optics Inc. (AMO)

Recalled Item: SENSAR 1-Piece IOL Recalled by Abbott Medical Optics Inc. (AMO) Due to...

The Issue: Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2016· Abbott Medical Optics Inc. (AMO)

Recalled Item: TECNIS 1-Piece IOL Recalled by Abbott Medical Optics Inc. (AMO) Due to...

The Issue: Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2016· Abbott Medical Optics Inc. (AMO)

Recalled Item: TECNIS Multifocal 1-Piece Intraocular Lens Recalled by Abbott Medical Optics...

The Issue: Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2016· Abbott Medical Optics Inc. (AMO)

Recalled Item: TECNIS Multifocal Foldable Acrylic Intraocular Lens Recalled by Abbott...

The Issue: Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they...

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

Class II — Potential Health HazardOngoing