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. 2,658 recalls have been distributed to New Jersey in the last 12 months.
Showing 24441–24460 of 53,621 recalls
Recalled Item: Curved Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to The...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Curved Intraluminal Stapler Recalled by Ethicon Endo-Surgery Inc...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straight Intraluminal Staplers Recalled by Ethicon Endo-Surgery Inc Due to...
The Issue: The staplers may have an insufficient firing stroke to break the washer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution Recalled by NxStage Medical, Inc. Due to Mislabeling
The Issue: Certain lots were mislabeled with incorrect product number.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MaxZero Extension Sets with Needle-less Connector Recalled by Becton...
The Issue: BD has decided to initiate a voluntary recall due to a confirmed complaint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neurovascular Recalled by Stryker Neurovascular Due to The firm has...
The Issue: The firm has become aware of a potential problem that their Catheters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProACT Implantation Instrument Set Recalled by Uromedica Inc. Due to...
The Issue: Potential issue with the manufacture and inspection of U-channel sheaths in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neurovascular Recalled by Stryker Neurovascular Due to The firm has...
The Issue: The firm has become aware of a potential problem that their Catheters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lamb s Supreme Potato Tater Puffs Recalled by Lamb Weston BSW LLC Due to...
The Issue: Formed Potato Tater Puffs (H30 s), sold as a foodservice item, are recalled...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cepheid Xpert SA Nasal Complete Control Panel (Catalog #8196) UDI: Recalled...
The Issue: Product with incorrect shelf life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q (material 10848280 Recalled by Siemens Medical Solutions USA, Inc...
The Issue: In affected Artis systems the movement of the floating tabletop may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Zeego (material 10280959) - Product Usage: AXIOM Artis zee Recalled by...
The Issue: In affected Artis systems the movement of the floating tabletop may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q (material 10848280 Recalled by Siemens Medical Solutions USA, Inc...
The Issue: In affected Artis systems the movement of the floating tabletop may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cepheid Xpert MRSA/MRSA NxG Control Panel (Catalog #8195) UDI:...
The Issue: Product with incorrect shelf life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Zee (material # 10094135 Recalled by Siemens Medical Solutions USA,...
The Issue: In affected Artis systems the movement of the floating tabletop may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 250 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Potential negative drift in Creatine Kinase (CK) results when used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediPress pneumatic compression system Full Arm (Medium)-Segmental Gradient...
The Issue: Product design change did not receive proper premarket clearance and lacks a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediPress pneumatic compression system Full Arm (Short)-Segmental Gradient...
The Issue: Product design change did not receive proper premarket clearance and lacks a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediPress pneumatic compression system Full Leg (Long)-Segmental Gradient...
The Issue: Product design change did not receive proper premarket clearance and lacks a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediPress pneumatic compression system Full Leg (Medium)-Segmental Gradient...
The Issue: Product design change did not receive proper premarket clearance and lacks a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.