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. 960 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
960 in last 12 months

Showing 48761–48780 of 53,528 recalls

Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Medline Steam Biological Indicators Recalled by Steritec Products Mfc. Co.,...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Zimmer, Inc.

Recalled Item: Persona (TM) The Personalized Knee System PS Tibial Articular Surface...

The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Mesa Labs Smart-Read 10^5 EZ Test BI Test Pack Recalled by Steritec Products...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Staar Surgical Co.

Recalled Item: nanoFLEX CC4204A Intraocular Lens Correct aphakia in persons 60 years...

The Issue: STAAR Surgical Company is recalling a limited number of nanoFLEX CC4204A and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Zimmer, Inc.

Recalled Item: Persona (TM) The Personalized Knee System CR Tibial Articular Surface...

The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Zimmer, Inc.

Recalled Item: Persona (TM) The Personalized Knee System UC Tibial Articular Surface...

The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Getinge Assure Accufast BI Test Pack w/ 25 Controls Recalled by Steritec...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Biomet 3i, LLC

Recalled Item: Osseotite Parallel Walled Certain 4mm(D)X 15mm (L) Dental Implant Product...

The Issue: One of the dental implants do not have the internal hex feature. One of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Zimmer, Inc.

Recalled Item: Persona (TM) The Personalized Knee System Tibial Articular Surface...

The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Getinge Assure Accufast BI Test Pack w/ 5 Controls Recalled by Steritec...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2013· Steritec Products Mfc. Co., Inc.

Recalled Item: Medline Med-Checks BI Test packs with Instant Readout Integrator Recalled by...

The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...

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

Class II — Potential Health HazardOngoing
FoodJune 10, 2013· Nassau Candy

Recalled Item: PISTACHIOS-INSHELL-R/S-21/25-6.25LB Recalled by Nassau Candy Due to...

The Issue: Potential Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 7, 2013· Sequel Naturals Ltd

Recalled Item: vega sport Recalled by Sequel Naturals Ltd Due to Raw material supplier of...

The Issue: Raw material supplier of the chocolate used for the bar coating had milk...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 7, 2013· Sequel Naturals Ltd

Recalled Item: vega sport Recalled by Sequel Naturals Ltd Due to Raw material supplier of...

The Issue: Raw material supplier of the chocolate used for the bar coating had milk...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 7, 2013· Sequel Naturals Ltd

Recalled Item: vega one Recalled by Sequel Naturals Ltd Due to Raw material supplier of the...

The Issue: Raw material supplier of the chocolate used for the bar coating had milk...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 7, 2013· Sequel Naturals Ltd

Recalled Item: vega one Recalled by Sequel Naturals Ltd Due to Raw material supplier of the...

The Issue: Raw material supplier of the chocolate used for the bar coating had milk...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 7, 2013· Sequel Naturals Ltd

Recalled Item: vega one Recalled by Sequel Naturals Ltd Due to Raw material supplier of the...

The Issue: Raw material supplier of the chocolate used for the bar coating had milk...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00595202010 Articular Surface XLPE CR ART SURF 1 Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597103110 Provisional CR ART SURF PROV 34/STR YEL 10 Recalled by Zimmer,...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00595204110 Articular Surface XLPE CR ART SURF 5-6/STRGRN 10 Recalled by...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing