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 31341–31360 of 53,621 recalls
Recalled Item: IQon Spectral CT (Model No. 728332) Recalled by Philips Medical Systems...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT SP (Model No. 728311 Recalled by Philips Medical Systems...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT (Model No. 728326) Recalled by Philips Medical Systems...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 (Model No. 728323) Recalled by Philips Medical Systems...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore Radiology CT (Model No. 728244) software version...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 (Model No. 728231) Recalled by Philips Medical Systems...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore Oncology CT (Model No. 728243) software version Recalled...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core (Model No. 728321) Recalled by Philips Medical Systems...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALE HOUSE BEER BATTERED 3/8 ONION RINGS - NET WT. Recalled by Oxford Frozen...
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Small White Button Mushroom Regular Batter: ATLANTIC GOLD Battered Mushrooms...
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 5/8" Thick Cut Beer Battered Onion Rings: ALE HOUSE BEER Recalled by Oxford...
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Thin Cut Regular Batter: BLUE ACRES BATTERED ONION RINGS Recalled by Oxford...
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 33034 33116 Thick Cut Regular Batter: ATLANTIC GOLD STEAK CUT Recalled by...
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1/2" Thick Cut Beer Battered Onion Rings: ALE HOUSE BEER Recalled by Oxford...
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Artis Zee and Zeego Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for liquid entry
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectranetics Turbo-Elite Laser Atherectomy Catheter Peripheral Rapid...
The Issue: Potential for flouroscopially visible marker band at the tip of the Rapid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q and Q.Zen Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for liquid entry
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NasalCrom (cromolyn sodium) Nasal Spray Recalled by Bausch & Lomb, Inc. Due...
The Issue: CGMP Deviations: Possibility of the presence of microbial contamination in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Helix Elite" Molecular Standards: Inactivated Standard. Inactivated...
The Issue: Real-time shelf life testing failed at 24 months
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbiologics QC Sets and Panels: Helix Elite. Extended Enteric Bacterial...
The Issue: Real-time shelf life testing failed at 24 months
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.