Product Recalls in Arizona

Product recalls affecting Arizona — including food, drugs, consumer products, medical devices, and vehicles distributed to Arizona. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,122 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
1,122 in last 12 months

Showing 8441–8460 of 52,339 recalls

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
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: 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· 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) 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): 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
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· 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: CLP Hip 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· 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: 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
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· 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 3, 2023· LivaNova Deutschland GmbH

Recalled Item: 3T Heater Cooler System Recalled by LivaNova Deutschland GmbH Due to The...

The Issue: The firm's labeling (Quick Guide) contains incorrect information in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE STERILE IRIS SCISSORS CVD/STD Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: 4.5" Iris Scissors, Sterile, Curved (DYNJ04049) are being recalled due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2023· Accuray Incorporated

Recalled Item: Upper roller bracket (part number 1088370) for the Gen2 gantry Recalled by...

The Issue: It is possible the upper roller bracket in the Radixact System gantry...

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

Class II — Potential Health HazardOngoing