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. 2,743 recalls have been distributed to New Jersey in the last 12 months.
Showing 17581–17600 of 29,496 recalls
Recalled Item: TunneLoc Tibial Fixation Device (Within an ACL Kit) Product Usage: Recalled...
The Issue: Gamma sterilization validation testing indicates the sterilization dose for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TunneLoc Tibial Fixation Device Product Usage: To provide fixation of...
The Issue: Gamma sterilization validation testing indicates the sterilization dose for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestation 620 A2 Recalled by GE Medical Systems China Co., Ltd. Due to...
The Issue: Possible incomplete seal between the CO2 absorber and the breathing circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crimson Trace Corporation laser sights. The Finished Products are laser...
The Issue: A previously "in specification" Finished Product with a Model 25-0657 diode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE DOUBLE SWIVEL CLOSED SUCTION CATHETER Recalled by Medline Industries...
The Issue: Products labeled as sterile were distributed prior to sterilization
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STORZ High Flow Insufflation Tubing (with filter) Recalled by Karl Storz...
The Issue: The label outside the cardboard box is labeled correctly but the pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE PEDI ELBOW CLOSED SUCTION CATHETER Recalled by Medline Industries...
The Issue: Products labeled as sterile were distributed prior to sterilization
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect Legacy(TM) 3 Implant Recalled by Implant Direct Sybron...
The Issue: One reported complaint and discovered that the outer vial was out of round...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...
The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...
The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults with BALLARD Technology WET...
The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...
The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Closed Suction System for Adults Recalled by Halyard Health, Inc Due...
The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOVAPLUS* Endotracheal WET PAK* Closed Suction System for Adults with...
The Issue: Received recall notification from Smiths Medical that lots of 15ml Saline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical 2 MHZ Waterproof OB Probe Product The CooperSurgical...
The Issue: The 2MHZ prove was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiolucent Surgery Spine Frame (F70801). Surgical platform used to position...
The Issue: The base of the frame has the potential to crack when the patient is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allen Medical Bow Frame Model A-70800. Surgical platform used to Recalled by...
The Issue: The base of the frame has the potential to crack when the patient is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.