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. 2,577 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,577 in last 12 months

Showing 2192121940 of 53,528 recalls

Medical DeviceAugust 15, 2019· Normand-Info S.A.S.U.

Recalled Item: Remisol Advance running on hardware with Windows XP Recalled by Normand-Info...

The Issue: A patch was released for a critical remote code execution vulnerability in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Western / Scott Fetzer Company

Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9615 Recalled by Western /...

The Issue: Limited access to flow settings as a result of the control knob having been...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Western / Scott Fetzer Company

Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9627 Recalled by Western /...

The Issue: Limited access to flow settings as a result of the control knob having been...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Western / Scott Fetzer Company

Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9653 Recalled by Western /...

The Issue: Limited access to flow settings as a result of the control knob having been...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Western / Scott Fetzer Company

Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9646 Recalled by Western /...

The Issue: Limited access to flow settings as a result of the control knob having been...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2019· Western / Scott Fetzer Company

Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9632 Recalled by Western /...

The Issue: Limited access to flow settings as a result of the control knob having been...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2019· Bard Peripheral Vascular Inc

Recalled Item: Bard Conquest 40 PTA Dilation Catheter Recalled by Bard Peripheral Vascular...

The Issue: The catheter packaging incorrectly listed the balloon size as 8mm X 20mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2019· WOM World of Medicine AG

Recalled Item: Aquilex Fluid Control System component: Bag deflector Recalled by WOM World...

The Issue: The deficit displayed by the pump can differ from the real deficit, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2019· Siemens Healthcare Diagnostics, Inc

Recalled Item: Atellica IM anti-CCP IgG (aCCP) Assay Siemens Material Number: 10732998...

The Issue: Atellica IM anti-CCP IgG (aCCP) Test Definition (TDef) Mitigation...

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

Class II — Potential Health HazardOngoing
DrugAugust 14, 2019· Pfizer Inc.

Recalled Item: RELPAX (eletriptan HBr) tablets Recalled by Pfizer Inc. Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: contamination with...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 13, 2019· Ethicon, Inc.

Recalled Item: STRATAFIX Spiral PDS Plus Violet 27 (70cm) CTX Needle Product Recalled by...

The Issue: The product does not meet certain internal strength testing specifications.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2019· Baxter Healthcare Corporation

Recalled Item: EXACTAMED Oral Dispensers Recalled by Baxter Healthcare Corporation Due to...

The Issue: Exactamed 5 mL Oral Dispenser Pharmacy Packs may contain both 5 mL and 3 mL...

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: AssayTip/AssayCup Tray-used on the cobas e 801 module which is Recalled by...

The Issue: AssayTips part of the AssayTip/AssayCup Tray Tips used on the cobas e 801...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2019· Ethicon, Inc.

Recalled Item: STRATAFIX Spiral PDS Plus Violet 18 (45cm) CT-1 Needle Product Recalled by...

The Issue: The product does not meet certain internal strength testing specifications.

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

Class II — Potential Health HazardOngoing
DrugAugust 12, 2019· First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Recalled Item: S-VIT B COMPLEX (1/3/5/6/12A) MDV INJ 100/2/2/100/1MG/ML Recalled by First...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 12, 2019· First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Recalled Item: S-METHYLCOBALAMIN 10 Recalled by First Royal Care Co. LLC, dba Red Mountain...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 12, 2019· First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Recalled Item: S-E2/TEST CYP 0.4MG/1MG/MLMDV IN OIL INJECTION Recalled by First Royal Care...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 12, 2019· First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Recalled Item: S-HCG/B12A 1000U/5MG/ML MDV INJ Recalled by First Royal Care Co. LLC, dba...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 12, 2019· First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Recalled Item: S-HYDROXOCOBALAMIN 1000MCG/ML MDV INJ Recalled by First Royal Care Co. LLC,...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 12, 2019· First Royal Care Co. LLC, dba Red Mountain Compounding Pharmacy

Recalled Item: S-DEXTROSE 50% MDV SOLN Recalled by First Royal Care Co. LLC, dba Red...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund