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 3574135760 of 55,415 recalls

Medical DeviceJuly 29, 2016· Zyno Medical LLC

Recalled Item: Zyno Medical Administration Set Recalled by Zyno Medical LLC Due to...

The Issue: Administration Set potential filter leaking

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2016· Zyno Medical LLC

Recalled Item: Zyno Medical Administration Set Recalled by Zyno Medical LLC Due to...

The Issue: Administration Set potential filter leaking

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

Class II — Potential Health HazardOngoing
FoodJuly 28, 2016· Gel Spice Co, Inc.

Recalled Item: 1) Ground Tumeric item #73535 Net Wt 50 lbs Distributed by Gel Spice Co....

The Issue: Ground Turmeric may contain excess levels of lead.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 28, 2016· Handicare AB

Recalled Item: Carina Mobile Lifts Recalled by Handicare AB Due to A limited amount of...

The Issue: A limited amount of Carina mobile lifts have been delivered with a too small...

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

Class II — Potential Health HazardOngoing
DrugJuly 27, 2016· Akorn, Inc.

Recalled Item: Desoximetasone Gel USP Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: product was out of...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 27, 2016· OrthoPediatrics Corp

Recalled Item: 3.5mm Bowed Locking Compression Femur Plates Recalled by OrthoPediatrics...

The Issue: OrthoPediatrics Corp.is voluntarily recalling multiple lots of the 3.5mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2016· OrthoPediatrics Corp

Recalled Item: 3.5mm Bowed Locking Compression Femur Plates Recalled by OrthoPediatrics...

The Issue: OrthoPediatrics Corp.is voluntarily recalling multiple lots of the 3.5mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2016· INNOKAS MEDICAL OY

Recalled Item: CARESCAPE VC150 Vital Signs Monitor Recalled by INNOKAS MEDICAL OY Due to A...

The Issue: A software error on released software versions 1.6.12, 1.6.12F and 1.6.16...

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

Class II — Potential Health HazardOngoing
FoodJuly 26, 2016· La Torre Foods Usa, Inc.

Recalled Item: la Torre Copito Marshmallow Chocolate Cookie NET WT 4.94 oz Recalled by La...

The Issue: Calcium caseinate is declared on the label, but milk is not listed.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 26, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo RT Therapist Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Software patch installation to address several safety issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: PRIMUS Recalled by Siemens Medical Solutions USA, Inc Due to Software patch...

The Issue: Software patch installation to address several safety issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: ARTISTE Recalled by Siemens Medical Solutions USA, Inc Due to Software patch...

The Issue: Software patch installation to address several safety issues.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Howmedica Osteonics Corp.

Recalled Item: AccuLIF PL 8-12mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...

The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Howmedica Osteonics Corp.

Recalled Item: AccuLIF PL 10-16mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...

The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Howmedica Osteonics Corp.

Recalled Item: AccuLIF PL 6-9mm x 11mm x 27mm x 8 Cage Recalled by Howmedica Osteonics...

The Issue: Since Stryker acquired the AccuLIF product in March of 2014, there have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Encore Medical, Lp

Recalled Item: Cobalt HV Bone Cement Product Usage: Cobalt HV Bone Cement Recalled by...

The Issue: The outer packaging was mislabeled on the box indicating "Cobalt HV with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2016· Philips Electronics North America Corporation

Recalled Item: IntelliVue Patient Monitor Product Usage: The monitors are indicated for...

The Issue: If an affected Patient Monitor has been powered on continuously for several...

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

Class II — Potential Health HazardOngoing
FoodJuly 25, 2016· SK Food Group Groveport

Recalled Item: Slow Roasted Ham & Swiss Breakfast Sandwich Recalled by SK Food Group...

The Issue: The product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 25, 2016· Meijer Distribution, Inc

Recalled Item: MEIJER MACARONI SALAD 1 LB. plastic retail container Recalled by Meijer...

The Issue: salads and sandwiches contain a sourced cooked egg ingredient which tested...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 25, 2016· Meijer Distribution, Inc

Recalled Item: MARKETS OF MEIJER SALAD SEASHELL MACARONI Food service Recalled by Meijer...

The Issue: salads and sandwiches contain a sourced cooked egg ingredient which tested...

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

Class I — Serious Health HazardOngoing
Refund