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. 2,697 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,697 in last 12 months

Showing 1256112580 of 53,528 recalls

FoodMay 20, 2022· The JM Smucker Company LLC

Recalled Item: JIF REDUCED FAT CREAMY PEANUT BUTTER packaged in 16oz and 40oz Recalled by...

The Issue: Products are potentially contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 20, 2022· The JM Smucker Company LLC

Recalled Item: JIF 1.5 oz CRUNCHY PEANUT BUTTER TO GO packaged in 8 count cases Recalled by...

The Issue: Products are potentially contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 20, 2022· The JM Smucker Company LLC

Recalled Item: JIF CRUNCHY PEANUT BUTTER packaged in 500 gram Recalled by The JM Smucker...

The Issue: Products are potentially contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 20, 2022· The JM Smucker Company LLC

Recalled Item: JIF NATURAL CREAMY PEANUT BUTTER packaged in 16oz Recalled by The JM Smucker...

The Issue: Products are potentially contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 20, 2022· The JM Smucker Company LLC

Recalled Item: JIF DARK ROAST CREMY PEANUT BUTTER packaged in 500 gram and 1 kilogram...

The Issue: Products are potentially contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 20, 2022· The JM Smucker Company LLC

Recalled Item: JIF 1.5 oz NATURAL CREAMY PEANUT BUTTER TO GO packaged in 8 and 36 count...

The Issue: Products are potentially contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 20, 2022· Morski Brands, Inc.

Recalled Item: Ranch BLT Pasta Salad Recalled by Morski Brands, Inc. Due to Foreign Object...

The Issue: Foreign object (metal).

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 20, 2022· The JM Smucker Company LLC

Recalled Item: JIF 1.5 oz and 31.25 gram CREAMY PEANUT BUTTER TO GO packaged in 3 Recalled...

The Issue: Products are potentially contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 20, 2022· ROi CPS LLC

Recalled Item: regard Item Number: 800774001 Recalled by ROi CPS LLC Due to A nonsterile...

The Issue: A nonsterile component was packaged in a sterile convenience kit.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2022· Agilent Technologies, Inc.

Recalled Item: Kit Label: Anti-FITC-AP CISH Accessory Kit (Dako Omnis) Recalled by Agilent...

The Issue: Label provided for substrate vail contained incorrect expiration date.

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

Class III — Low RiskOngoing
Medical DeviceMay 20, 2022· DePuy Spine, Inc.

Recalled Item: EIT CIF cage Recalled by DePuy Spine, Inc. Due to Label on the Outer Carton...

The Issue: Label on the Outer Carton does not match the labels on the Outer Blister...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2022· Menarini Silicon Biosystems

Recalled Item: CELLSEARCH Circulating Tumor Cell Kit (Epithelial)-IVD intended for the...

The Issue: High number of total images/unassigned events including (dual positives) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2022· Cordis US Corp

Recalled Item: PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System...

The Issue: Potential for stent dislodgement and associated failures related to two...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Icono Recalled by Siemens Medical Solutions USA, Inc Due to During...

The Issue: During system tests, an increased wearing of the Image acquisition system...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2022· Draeger Medical Systems, Inc.

Recalled Item: Draeger Globe-Trotter and Globe-Trotter IC Recalled by Draeger Medical...

The Issue: The firm has initiated this recall to replace component on devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2022· DePuy Spine, Inc.

Recalled Item: EIT CIF cage Recalled by DePuy Spine, Inc. Due to Label on the Outer Carton...

The Issue: Label on the Outer Carton does not match the labels on the Outer Blister...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2022· C.R. Bard Inc

Recalled Item: Sensica Urine Output System Recalled by C.R. Bard Inc Due to Complaints...

The Issue: Complaints relating to urine output measurement accuracy.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension LTNI -In vitro diagnostic test intended to quantitively measure...

The Issue: Positive bias with Lithium Heparin plasma samples from individuals that are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2022· Radiometer Medical ApS

Recalled Item: ABL800 Flex Analyzer Model Numbers 393-800 and 393-801 Recalled by...

The Issue: There is a potential for sporadic incidents of positive and negative biases...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 18, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension CTNI-In vitro diagnostic test intended to quantitively measure...

The Issue: Positive bias with Lithium Heparin plasma samples from individuals that are...

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

Class II — Potential Health HazardOngoing