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. 1,895 recalls have been distributed to New Jersey in the last 12 months.
Showing 30721–30740 of 53,621 recalls
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 5% Dextrose Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 5% Dextrose Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 5% Dextrose Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection 20 mMol in Recalled by...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Succinylcholine Chloride Injection (Preserved) 20 mg per mL Recalled by...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection 15 mMol in Recalled by...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium PHOSphate in 5% Dextrose Injection Recalled by PharMedium...
The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Stroke Fast Pack(TM) Trevo XP ProVue Retriever 3 x 20 Recalled by Stryker...
The Issue: Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere iScreen Dx Urine Drug Screen Card Recalled by Ameditech Inc Due to The...
The Issue: The kit box label incorrectly identifies PCP (instead of TCA) as one of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Burn Sheet Recalled by Certified Safety Mfg Inc Due to Burn Sheet has...
The Issue: Burn Sheet has possibility of being shredded.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coulter LH 750 Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...
The Issue: Beckman Coulter has determined that additional clarification for the Blast...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 20 Recalled by Stryker...
The Issue: Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 30 Recalled by Stryker...
The Issue: Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt HV with Gentamicin Recalled by Encore Medical, Lp Due to Loss of the...
The Issue: Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.