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. 2,455 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,455 in last 12 months

Showing 5090150920 of 53,528 recalls

Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS R 9IN CALC 2.25/22.5 Packaging: Product is packed Recalled by DePuy...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS F 9 CALC L 13.5MM LG Packaging: Product Recalled by DePuy...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS L 9IN CALC 2.25/16.5 Packaging: Product is packed Recalled by DePuy...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS 8IN CALCAR SZ12 Packaging: Product is packed within a poly protector...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
DrugNovember 30, 2012· West-ward Pharmaceutical Corp.

Recalled Item: Carisoprodol Tablets Recalled by West-ward Pharmaceutical Corp. Due to...

The Issue: Labeling: Not elsewhere classified: On 12/12/11, DEA published a final rule...

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

Class III — Low RiskOngoing
Refund
DrugNovember 30, 2012· West-ward Pharmaceutical Corp.

Recalled Item: Lisinopril and Hydrochlorothiazide Tablets Recalled by West-ward...

The Issue: Presence of Foreign Substance: Reports of gray smudges identified as minute...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 30, 2012· Unified Grocers Inc.

Recalled Item: Pure Apricot Pecan Flats Recalled by Unified Grocers Inc. Due to Undeclared...

The Issue: Unified Grocers is recalling Pure Apricot Pecan Flats because it may contain...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 30, 2012· Biomet Spine, LLC

Recalled Item: Set Screw 5.5 mm Rod - Model #7703-1600. Product Usage: Recalled by Biomet...

The Issue: Biomet Spine LLC is recalling the Set Screw 5.5 mm Rod due to the set screw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2012· St. Jude Medical

Recalled Item: Eon and Eon Mini charging system Recalled by St. Jude Medical Due to There...

The Issue: There is issues of warmth or heating at the implant site during charging for...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2012· Handicare Accessibility

Recalled Item: Handset component of the Handicare USA's Minivator Bath Bliss Reclining...

The Issue: Firm became aware that two handsets in the affected batches became...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2012· Thermo Fisher Scientific (Asheville) LLC

Recalled Item: CO2 Incubators (General Purpose Incubator) Recalled by Thermo Fisher...

The Issue: Incubators manufactured prior to mid 2009 have coated metal hinges that have...

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

Class II — Potential Health HazardOngoing
FoodNovember 28, 2012· Williams West & Witt's Products Company

Recalled Item: #326 RS PrimarqueLobster Base Recalled by Williams West & Witt's Products...

The Issue: The ingredient label did not identify the source of butter and cream...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 28, 2012· Williams West & Witt's Products Company

Recalled Item: #222-C Recalled by Williams West & Witt's Products Company Due to The...

The Issue: The ingredient label did not identify the source of butter and cream...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 28, 2012· Williams West & Witt's Products Company

Recalled Item: #828 Cook's Delight Shrimp Base Recalled by Williams West & Witt's Products...

The Issue: The ingredient label did not identify the source of butter and cream...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 28, 2012· Williams West & Witt's Products Company

Recalled Item: #126 Primarque Seafood Base Recalled by Williams West & Witt's Products...

The Issue: The ingredient label did not identify the source of butter and cream...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 28, 2012· Williams West & Witt's Products Company

Recalled Item: #272N Cook's Delight Mushroom Base Recalled by Williams West & Witt's...

The Issue: The ingredient label did not identify the source of butter and cream...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 28, 2012· Williams West & Witt's Products Company

Recalled Item: #425N Primarque Fish Base Recalled by Williams West & Witt's Products...

The Issue: The ingredient label did not identify the source of butter and cream...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 28, 2012· Williams West & Witt's Products Company

Recalled Item: #223-E Primarque Clam Base Recalled by Williams West & Witt's Products...

The Issue: The ingredient label did not identify the source of butter and cream...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 28, 2012· Williams West & Witt's Products Company

Recalled Item: #122-A Recalled by Williams West & Witt's Products Company Due to The...

The Issue: The ingredient label did not identify the source of butter and cream...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 28, 2012· Williams West & Witt's Products Company

Recalled Item: #321N Primarque Crab Base Recalled by Williams West & Witt's Products...

The Issue: The ingredient label did not identify the source of butter and cream...

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

Class II — Potential Health HazardOngoing
Refund