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. 2,642 recalls have been distributed to New Jersey in the last 12 months.
Showing 29261–29280 of 53,621 recalls
Recalled Item: 0.25% Acetic Acid Irrigation USP Recalled by B. Braun Medical Inc Due to...
The Issue: Presence of Particulate Matter: identified as polyethylene, which is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fosphenytoin Sodium Injection Recalled by Amneal Pharmaceuticals Due to...
The Issue: Presence of particulate matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BrightView XCT Model 882482 Product Usage: BrightView XCT is a Recalled by...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precedence 16 Model # 882350 Product Usage: Precedence (cleared as Recalled...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView Model 882480 Product Usage: BrightView and BrightView X are...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precedence 6 Model # 882351 Product Usage: Precedence (cleared as Recalled...
The Issue: During collimator exchange, the alignment of the collimator cart and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vado Bi-Directional Steerable Sheath 8.8F Recalled by Kalila Medical Due to...
The Issue: Torn sheath liner material was detected at the proximal end of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vado Steerable Sheath 8.8F Recalled by Kalila Medical Due to Torn sheath...
The Issue: Torn sheath liner material was detected at the proximal end of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shiseido Future Solutions LX Triple Points Bonus contains SPF 50+ Recalled...
The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shiseido Future Solution LX Discovery Set contains SPF 50+ (octinoxate 4.9%...
The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Moexipril Hydrochloride and Hydrocholorothiazide Tablets USP Recalled by...
The Issue: Failed Impurities/Degradation Specifications: High out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shiseido Future Solution LX Luxurious Eye & Lip Collection contains Recalled...
The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SPIRIVA HandiHaler (tiotropium bromide inhalation powder) 18 mcg/capsule (90...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: bareMinerals Broad Spectrum SPF 50 Daily Prep Lotion (zinc oxide 23.8%...
The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shiseido Future Solution LX Universal Defense SPF 50+ (octinoxate 4.9%...
The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ARCHITECT DHEA-S Reagent Product Usage: It is a chemiluminescent...
The Issue: Falsely elevated results may be obtained when using the ARCHITECT DHEA-S...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signia" Power Handle (SIGPHANDLE Recalled by Covidien LLC Due to Product...
The Issue: Product reportedly shutting down during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORTRAK* 2 Nasogastric/Nasointestinal (NG/NI) Feeding Tubes with...
The Issue: The transmitting stylet within CORTRAK* 2 nasogastric/Nasointestinal (NG/NI)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 365 brand Egg Nog Recalled by Harrisburg Dairies, Inc Due to Dried Egg Yolks...
The Issue: Dried Egg Yolks was not specifically stated in ingredient statement
Recommended Action: Do not consume. Return to store for a refund or discard.