Product Recalls in Ohio

Product recalls affecting Ohio — including food, drugs, consumer products, medical devices, and vehicles distributed to Ohio. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,542 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,542 in last 12 months

Showing 3754137560 of 55,415 recalls

Medical DeviceMarch 24, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Computed Tomography X-ray systems is intended to produce...

The Issue: Software defect causing intermittently slow response of Host.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Abbott Laboratories

Recalled Item: The ARCHITECT Estradiol Kit Intended to measure estradiol Recalled by Abbott...

The Issue: Interaction of Fulvestrant with the ARCHITECT Estradiol assay, leading to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Siemens Healthcare Diagnostics Inc.

Recalled Item: Dimension Vista 500 Intelligent Lab System running on software versions...

The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Siemens Healthcare Diagnostics Inc.

Recalled Item: Dimension Vista 1500 Intelligent Lab System running on software versions...

The Issue: Discrepant patient results on Dimension Vista Intelligent Lab Systems....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· CareFusion 303, Inc.

Recalled Item: Alaris PC unit Recalled by CareFusion 303, Inc. Due to The Alaris PC units...

The Issue: The Alaris PC units model 8015 may display a system error code 133.6080 due...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Philips and Neusoft Medical Systems Co., Ltd.

Recalled Item: NeuViz 16 Multi-Slice CT Scanner System PN: 989605858501 a whole Recalled by...

The Issue: The following issues are found in NeuViz 16 systems with software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2016· Abbott Laboratories

Recalled Item: CELL-DYN Emerald Cleaner Recalled by Abbott Laboratories Due to Three lots...

The Issue: Three lots of CELL-DYN Emerald Cleaner may have occurrences where the...

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

Class II — Potential Health HazardOngoing
DrugMarch 23, 2016· Hospira Inc.

Recalled Item: Magnesium Sulfate Inj. Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Confirmed customer complaint for the...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 23, 2016· Akorn, Inc.

Recalled Item: Chlorhexidine gluconate Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: Out-of-specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2016· Akorn, Inc.

Recalled Item: PerioRx (chlorhexidine gluconate) Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: Out-of-specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2016· Akorn, Inc.

Recalled Item: ORIS (chlorhexidine gluconate) Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: Out-of-specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2016· TMIG Inc

Recalled Item: Renovo Patch (Capsaicin Recalled by TMIG Inc Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA: product is an unapproved drug and...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2016· Hospira Inc.

Recalled Item: Magnesium Sulfate Inj. Recalled by Hospira Inc. Due to Failed pH...

The Issue: Failed pH Specifications: Confirmed high out of specification (OOS) results...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 23, 2016· Acumedia Manufacturers, Inc.

Recalled Item: Nutrient Gelatin Recalled by Acumedia Manufacturers, Inc. Due to Incorrect...

The Issue: Incorrect expiration date was listed on the label. Correct expiration date...

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

Class III — Low RiskOngoing
Medical DeviceMarch 22, 2016· Medscience Inc

Recalled Item: AllergiEnd ST-9 Multiple Skin Test Applicator (Item 1000) and AllergiEnd...

The Issue: During an FDA inspection it was found that the products are marketed without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2016· Leica Microsystems, Inc.

Recalled Item: Novocastra Liquid Mouse Monoclonal Antibody Calretinin Recalled by Leica...

The Issue: Novocastra Liquid Mouse Monoclonal Antibody Calretinin when used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2016· Boston Scientific Corporation

Recalled Item: Boston Scientific Fetch 2 Aspiration Catheter Recalled by Boston Scientific...

The Issue: Boston Scientific is recalling all models of Fetch 2 Aspiration Catheter as...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 22, 2016· Coloplast Manufacturing US, LLC

Recalled Item: Self-Cath¿ Pediatric Catheter Size CH 06 Recalled by Coloplast Manufacturing...

The Issue: Coloplast Corp. is voluntarily recalling a single lot of Self-Cath Pediatric...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Siemens became aware that the front cover on some Siemens CT system was not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2016· Windstone Medical Packaging, Inc.

Recalled Item: Laparotomy Pack Latex Free Recalled by Windstone Medical Packaging, Inc. Due...

The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...

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

Class II — Potential Health HazardOngoing