Product Recalls in New Jersey
Product recalls affecting New Jersey — including food, drugs, consumer products, medical devices, and vehicles distributed to New Jersey. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,862 recalls have been distributed to New Jersey in the last 12 months.
Showing 2861–2880 of 29,496 recalls
Recalled Item: SECURE 1000 mL EMPTY EVA CONTAINER With 2 Ports Recalled by The Metrix...
The Issue: A limited number of IV bags have been found to leak during filling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MONOCRYL" (poliglecaprone 25) Suture MONOCRYL" Sutures are indicated...
The Issue: Due a component mix-up in manufacturing, the affected products may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Approach Hydro ST Micro Wire Guide Recalled by Cook Incorporated Due to...
The Issue: Affected device lots have labels that state the incorrect expiration dates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Approach CTO Micro Wire Guide Recalled by Cook Incorporated Due to Affected...
The Issue: Affected device lots have labels that state the incorrect expiration dates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRG:HYBRiD-XL Insulin. Model/Catalog Number: HYE-5361 Recalled by DRG...
The Issue: The user of the assay may either face a failure message during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Universal Ventilator. Model Number DS2000X11B. Intended for...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EV300. Model Numbers: DS2200X11B Recalled by Philips Respironics,...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aeris EVO. Model Number: VT2110X24B. Intended for invasive and non-invasive...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Garbin Evo. Model Number: LD2110X23B. Intended for invasive and non-invasive...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeVent EVO2. Model Number: SP2100X26B. Intended for invasive and...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Zenition 50 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Potential for the Mains Control Unit board fuse may blow out during system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo O2. Model Numbers: FP2100X10 Recalled by Philips Respironics,...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo. Model Numbers: DS2110X11B Recalled by Philips Respironics, Inc....
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Zenition 70 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Potential for the Mains Control Unit board fuse may blow out during system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOMEMS HF PRESSURE MEASUREMENT SYSTEM CardioMEMSTM HF System Hosptial...
The Issue: As a result of a cloud data migration of Patient and Hospital Electronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOMEMS HF PRESSURE MEASUREMENT SYSTEM CardioMEMSTM HF System Patient...
The Issue: As a result of a cloud data migration of Patient and Hospital Electronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...
The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE FreeStyle Comfort portable oxygen concentrator Recalled by Caire, Inc....
The Issue: Potential failure of affected units to recharge the battery of the oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...
The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...
The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.