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.

53,621 total recalls
2,642 in last 12 months

Showing 2770127720 of 53,621 recalls

Medical DeviceJune 18, 2018· Zimmer Biomet, Inc.

Recalled Item: Connecting Bolt Recalled by Zimmer Biomet, Inc. Due to Product was...

The Issue: Product was manufactured from the incorrect material, which shows a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2018· Medline Industries Inc

Recalled Item: Endoscopic Cleaning Brush Recalled by Medline Industries Inc Due to There is...

The Issue: There is potential risk of brush detachment during cleaning. If brush...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJune 15, 2018· Validus Pharmaceuticals, Inc.

Recalled Item: Calcitriol Oral Solution Recalled by Validus Pharmaceuticals, Inc. Due to...

The Issue: Subpotency: lower than expected potency result was obtained at the 18 month...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJune 15, 2018· Validus Pharmaceuticals, Inc.

Recalled Item: Rocaltrol (calcitriol) Oral Solution Recalled by Validus Pharmaceuticals,...

The Issue: Subpotency: lower than expected potency result was obtained at the 18 month...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceJune 14, 2018· Maquet SAS

Recalled Item: VOLISTA StandOP Surgical Light Recalled by Maquet SAS Due to Certain VOLISTA...

The Issue: Certain VOLISTA StandOP Surgical Lights have been identified as having a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2018· Beekley Corporation

Recalled Item: O-SPOT Recalled by Beekley Corporation Due to There is a potential for...

The Issue: There is a potential for imaging artifact to mimic calcifications on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2018· Smith & Nephew, Inc.

Recalled Item: JOURNEY BCS Knee Conventional Polyethylene Inserts: 74023111 Recalled by...

The Issue: The data in the National Joint Registry of England, Wales and Northern...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2018· Beekley Corporation

Recalled Item: TomoSPOT Recalled by Beekley Corporation Due to There is a potential for...

The Issue: There is a potential for imaging artifact to mimic calcifications on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2018· Beekley Corporation

Recalled Item: S-SPOT Recalled by Beekley Corporation Due to There is a potential for...

The Issue: There is a potential for imaging artifact to mimic calcifications on...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2018· Smith & Nephew, Inc.

Recalled Item: JOURNEY BCS OXINIUM Knee Femoral Components Recalled by Smith & Nephew, Inc....

The Issue: The data in the National Joint Registry of England, Wales and Northern...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2018· Bard Medical Division

Recalled Item: Arctic Sun Temperature Management System Recalled by Bard Medical Division...

The Issue: An improper wiring connection on the chiller assembly may result in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2018· Smith & Nephew, Inc.

Recalled Item: Journey BCS Knee CoCr Femoral Components Recalled by Smith & Nephew, Inc....

The Issue: The data in the National Joint Registry of England, Wales and Northern...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2018· Leica Microsystems, Inc.

Recalled Item: Leica Biosystems HistoCore SPECTRA ST Recalled by Leica Microsystems, Inc....

The Issue: These devices have an incorrect specification against safety standard...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJune 13, 2018· LUPIN SOMERSET

Recalled Item: Equate ClearLAX Recalled by LUPIN SOMERSET Due to Labeling: Not Elsewhere...

The Issue: Labeling: Not Elsewhere Classified - A private label distributor noted...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJune 12, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: HYDROmorphone 1 mg/mL (HYDROmorphone HCL (USP) 30 mg Recalled by Avella of...

The Issue: Lack of Assurance of Sterility: Potential leakage of bags.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: Midazolam 0.5mg/mL (Midazolam HCL (USP) 50 mg Recalled by Avella of Deer...

The Issue: Lack of Assurance of Sterility: Potential leakage of bags.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: ePHEDrine Sulfate Recalled by Avella of Deer Valley, Inc. Store 38 Due to...

The Issue: Lack of Assurance of Sterility: Potential leakage of bags.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: Vancomycin 1.25gm in D5W 250 mL. ( Vancomycin HCL (USP) 1.25 gm Recalled by...

The Issue: Lack of Assurance of Sterility: Potential leakage of bags.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: HEPARIN 1 Recalled by Avella of Deer Valley, Inc. Store 38 Due to Lack of...

The Issue: Lack of Assurance of Sterility: Potential leakage of bags.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: EPINEPHrine (USP) 4 mg Recalled by Avella of Deer Valley, Inc. Store 38 Due...

The Issue: Lack of Assurance of Sterility: Potential leakage of bags.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund