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. 1,110 recalls have been distributed to New Jersey in the last 12 months.
Showing 13481–13500 of 29,496 recalls
Recalled Item: Compress Recalled by Zimmer Biomet, Inc. Due to Elevated levels of bacterial...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Copeland HA Resurfacing Head Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.0MM BALL NOSE GUIDE WIRE Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive HHR Tess Cleat Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GUIDE WIRE 2.2MM X 28IN Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System Recalled...
The Issue: Potential need for device replacement - Elective Replacement Indicator (ERI)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System Recalled...
The Issue: Potential need for device replacement - Elective Replacement Indicator (ERI)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20" 2-Needle 26-Gauge 6mm HlgH-Flo Subcutaneous Safety Needle Sets" Product...
The Issue: Mislabeled needle lengths
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...
The Issue: Flow cytometers, when used with specific tubes may experience excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. 01-1503-0032 (Adolescent Nail Attachment Bolt). Component of the...
The Issue: Binding can occur between the attachment bolt and intramedullary nail, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. 01-1501-0032 (Child Nail Attachment Bolt). Component of the...
The Issue: Binding can occur between the attachment bolt and intramedullary nail, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoPediatrics Adolescent attachment bolt used with the Pediatric Nailing...
The Issue: Interference can occur between the adolescent attachment bolt and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...
The Issue: Flow cytometers, when used with specific tubes may experience excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...
The Issue: Flow cytometers, when used with specific tubes may experience excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...
The Issue: Flow cytometers, when used with specific tubes may experience excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...
The Issue: Flow cytometers, when used with specific tubes may experience excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...
The Issue: Flow cytometers, when used with specific tubes may experience excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...
The Issue: Flow cytometers, when used with specific tubes may experience excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...
The Issue: Flow cytometers, when used with specific tubes may experience excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSLyric Flow Cytometer Recalled by Becton, Dickinson and Company, BD...
The Issue: Flow cytometers, when used with specific tubes may experience excessive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.