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. 1,146 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
1,146 in last 12 months

Showing 8721–8740 of 55,415 recalls

Medical DeviceAugust 8, 2023· GE Medical Systems Information Technologies Inc

Recalled Item: Prucka 3 Amplifiers Recalled by GE Medical Systems Information Technologies...

The Issue: A diode on the power supply of the Prucka 3 Amplifier used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2023· FX SHOULDER

Recalled Item: Centered Glenosphere w/Screw Recalled by FX SHOULDER Due to Centered...

The Issue: Centered glenosphere box may contain an eccentric glenosphere.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· Thoratec Corp.

Recalled Item: Heartmate 3 LVAS Implant Kit Recalled by Thoratec Corp. Due to Inability to...

The Issue: Inability to start and/or complete the coring procedure due to inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· B. Braun Medical, Inc.

Recalled Item: B. Braun NORM-JECT Luer Solo Recalled by B. Braun Medical, Inc. Due to The...

The Issue: The sterile blister packaging may be damaged, and sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· Stryker Corporation

Recalled Item: Stryker ACM (Advanced Cement Mixing): 180-Gram Cement Cartridge with...

The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· Stryker Corporation

Recalled Item: Stryker ACM (Advanced Cement Mixing) System: Break-Away Femoral Nozzle-...

The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· Stryker Corporation

Recalled Item: Stryker ACM (Advanced Cement Mixing) System: ACM Kit w/ Femoral Recalled by...

The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· Stryker Corporation

Recalled Item: Stryker ACM (Advanced Cement Mixing) System: ACM Kit w/ Femoral Recalled by...

The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· B. Braun Medical, Inc.

Recalled Item: B.Braun NORM-JECT Luer Lock Solo Recalled by B. Braun Medical, Inc. Due to...

The Issue: The sterile blister packaging may be damaged, and sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· Stryker Corporation

Recalled Item: Stryker ACM (Advanced Cement Mixing)System: ACM Kit w/ Femoral Breakaway...

The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· Stryker Corporation

Recalled Item: Stryker ACM (Advanced Cement Mixing)System: ACM Kit w/ Femoral Breakaway...

The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· Stryker Corporation

Recalled Item: Stryker ACM (Advanced Cement Mixing) System: ACM Kit w/ Femoral Recalled by...

The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...

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

Class II — Potential Health HazardOngoing
DrugAugust 7, 2023· Advanced Accelerator Applications USA, Inc.

Recalled Item: PLUVICTO 1 Recalled by Advanced Accelerator Applications USA, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: vials were labeled with...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 5, 2023· Ortho-Clinical Diagnostics, INc.

Recalled Item: VITROS XT Chemistry Products ALKP Slides Recalled by Ortho-Clinical...

The Issue: Samples containing high levels of ALKP (or an interfering substance) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2023· Ortho-Clinical Diagnostics, INc.

Recalled Item: VITROS XT Chemistry Products TBIL-ALKP Slides Recalled by Ortho-Clinical...

The Issue: Samples containing high levels of ALKP (or an interfering substance) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2023· Encore Medical, LP

Recalled Item: DJO Surgical: Delta Ceramic Femoral Head Recalled by Encore Medical, LP Due...

The Issue: Orthopedic device components were not subjected to final sterilization...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2023· Encore Medical, LP

Recalled Item: DJO Surgical: Altivate Reverse Recalled by Encore Medical, LP Due to...

The Issue: Orthopedic device components were not subjected to final sterilization...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2023· Encore Medical, LP

Recalled Item: DJO Surgical: Empowr Knee Recalled by Encore Medical, LP Due to Orthopedic...

The Issue: Orthopedic device components were not subjected to final sterilization...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: HUDSON RCI Addipak Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Product dispositioned for scrap for sterility failure investigation that was...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 4, 2023· Encore Medical, LP

Recalled Item: DJO Surgical: Reverse Shoulder System (RSP) Semi Humeral Socket Insert...

The Issue: Orthopedic device components were not subjected to final sterilization...

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

Class II — Potential Health HazardOngoing