Product Recalls in Delaware
Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,668 recalls have been distributed to Delaware in the last 12 months.
Showing 5641–5660 of 27,373 recalls
Recalled Item: ADVIA Chemistry Iron_2 (IRON_2) Reagents Recalled by Siemens Healthcare...
The Issue: There is a potential for a positive bias on Quality Control (QC) and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oculus Pentacam AXL Recalled by Oculus Optikgeraete GMBH Due to Their is a...
The Issue: Their is a potential that optical devices with insufficient anti- coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oculus Myopia Master Recalled by Oculus Optikgeraete GMBH Due to Their is a...
The Issue: Their is a potential that optical devices with insufficient anti- coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oculus Pentacam AXL Wave Recalled by Oculus Optikgeraete GMBH Due to Their...
The Issue: Their is a potential that optical devices with insufficient anti- coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: NOVAPLUS GAMMEX NON-LATEX PI GREEN Surgical gloves Recalled by Ansell...
The Issue: Some surgical glove sterile pouches were not completely sealed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
Recalled Item: GAMMEX NON-LATEX PI GREEN Surgical gloves Recalled by Ansell Healthcare...
The Issue: Some surgical glove sterile pouches were not completely sealed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.