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. 2,846 recalls have been distributed to New Jersey in the last 12 months.
Showing 3361–3380 of 29,496 recalls
Recalled Item: MiniMed 630G Insulin Pump Recalled by Medtronic MiniMed, Inc. Due to Insulin...
The Issue: Insulin pumps that have been dropped, bumped, or experienced physical impact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ Total Bilirubin (TBIL) Flex Reagent Cartridge Recalled by...
The Issue: During manufacturing, the last three tests from the 160 test flex of lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by Siemens...
The Issue: The potential for biased quality control (QC) and patient results when using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by...
The Issue: The potential for biased quality control (QC) and patient results when using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DR 800. Digital Radiography X-ray System. Recalled by Agfa N.V. Due to...
The Issue: Potential for the front lever chain of the DR 800 table to fail.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM CA 19-9 (250 Test)- In vitro diagnostic use Recalled by Siemens...
The Issue: Positive bias for some samples around the CA 19-9 upper limit of normal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.