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. 970 recalls have been distributed to New Jersey in the last 12 months.
Showing 47061–47080 of 53,621 recalls
Recalled Item: Cefazolin for Injection USP and Dextrose Injection USP Recalled by B. Braun...
The Issue: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9 % Sodium Chloride Injection USP in PAB 50 mL Recalled by B. Braun...
The Issue: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9 % Sodium Chloride Injection USP Recalled by B. Braun Medical Inc Due to...
The Issue: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefepime for Injections USP and Dextrose Injection USP Recalled by B. Braun...
The Issue: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefazolin for Injection USP and Dextrose Injections USP Recalled by B. Braun...
The Issue: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefoxitin for Injection and Dextrose Injection Recalled by B. Braun Medical...
The Issue: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Indus Invue Screws: IM71058-XX: 04.2mm Recalled by SpineFrontier, Inc. Due...
The Issue: Mismarked and unmarked screws
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Indus Invue Screws: IM71013-XX: Indus Screw04.0mm SelfDrilling. Used to...
The Issue: Mismarked and unmarked screws
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Indus Invue Screws: lM71059-XX: Indus Screw 04.2mm SelfDrilling. Used to...
The Issue: Mismarked and unmarked screws
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 26mm Rotatable Retrieval Device (Box of 5 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Indus Invue Screws: IM71016-XX: 04.5mm Recalled by SpineFrontier, Inc. Due...
The Issue: Mismarked and unmarked screws
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pro clear(R) 1 day Sphere (o mafilcon A) Recalled by CooperVision Inc. Due...
The Issue: Lots were labeled with incorrect expiration dates on secondary package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 22mm Rotatable Retrieval Device (Box of 10 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClearSight(TM) Toric 1 day (ocufilcon D) Recalled by CooperVision Inc. Due...
The Issue: Lots were labeled with incorrect expiration dates on secondary package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 22mm Rotatable Retrieval Device (Box of 1 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 26mm Rotatable Retrieval Device (Box of 1 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 26mm Rotatable Retrieval Device (Box of 10 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORCHESTRA/ORCHESTRA PLUS Programmer Recalled by Sorin Group Italia S.r.l....
The Issue: Sorin has voluntarily issued a notification to physicians related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 22mm Rotatable Retrieval Device (Box of 5 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.