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. 2,580 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,580 in last 12 months

Showing 2898129000 of 55,415 recalls

Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 1000 Recalled by Shippert Medical Technologies Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Merit Medical Systems, Inc.

Recalled Item: 1mL Medallion Syringes Are used to inject fluids into Recalled by Merit...

The Issue: Supplier manufacturing defect with the syringe plunger tip.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 2000 Recalled by Shippert Medical Technologies Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 100 Recalled by Shippert Medical Technologies Due to The...

The Issue: The pouch integrity of the sterile product can't be assured without a visual...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 250 Recalled by Shippert Medical Technologies Due to The...

The Issue: The pouch integrity of the sterile product can't be assured without a visual...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Perspective (Model 10495568) Recalled by Siemens Medical Solutions...

The Issue: A potential risk of unnecessary radiation exposure due to a software issue

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2018· Medline Industries Inc

Recalled Item: Medline 0.9 % Sodium Chloride Injection Recalled by Medline Industries Inc...

The Issue: Packaged with an incorrect overwrap.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Emotion 16 (10165977) Recalled by Siemens Medical Solutions USA, Inc...

The Issue: A potential risk of unnecessary radiation exposure due to a software issue

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Scope Power (Model 10967888) Recalled by Siemens Medical Solutions...

The Issue: A potential risk of unnecessary radiation exposure due to a software issue

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Perspective 16 (Model 10891666) Recalled by Siemens Medical...

The Issue: A potential risk of unnecessary radiation exposure due to a software issue

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Emotion 6 (Model 10165888) Recalled by Siemens Medical Solutions...

The Issue: A potential risk of unnecessary radiation exposure due to a software issue

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Scope ( Model 10967666) Recalled by Siemens Medical Solutions USA,...

The Issue: A potential risk of unnecessary radiation exposure due to a software issue

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Spirit(Model 10045692 ) Recalled by Siemens Medical Solutions USA,...

The Issue: A potential risk of unnecessary radiation exposure due to a software issue

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

Class II — Potential Health HazardOngoing
FoodFebruary 1, 2018· J F C International Inc

Recalled Item: Daisho Kimchi Hot Pot Soup Base Recalled by J F C International Inc Due to...

The Issue: Daisho Kimchi Hot Pot Soup base contains undeclared fish - shrimp and crab.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 1, 2018· Improper Goods

Recalled Item: Lemon Ginger Syrup Recalled by Improper Goods Due to Lemon Ginger Syrup is...

The Issue: Lemon Ginger Syrup is recalled because the internal fill temperature of this...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 1, 2018· Improper Goods

Recalled Item: Hibiscus Lavender Syrup Recalled by Improper Goods Due to Hibiscus Lavender...

The Issue: Hibiscus Lavender Syrup is recalled because the internal fill temperature...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 31, 2018· Cook Inc.

Recalled Item: StoneBreaker C02 Cartridge Recalled by Cook Inc. Due to The interior of the...

The Issue: The interior of the product may not be sterilized to the appropriate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2018· Cook Inc.

Recalled Item: StoneBreaker Probe Cap Recalled by Cook Inc. Due to The interior of the...

The Issue: The interior of the product may not be sterilized to the appropriate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2018· Cook Inc.

Recalled Item: StoneBreaker Exhaust Line Recalled by Cook Inc. Due to The interior of the...

The Issue: The interior of the product may not be sterilized to the appropriate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2018· Cook Inc.

Recalled Item: StoneBreaker Single Use Probe Recalled by Cook Inc. Due to The interior of...

The Issue: The interior of the product may not be sterilized to the appropriate...

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

Class II — Potential Health HazardOngoing