Product Recalls in Delaware

Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,457 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,457 in last 12 months

Showing 2600126020 of 27,373 recalls

Medical DeviceNovember 14, 2012· Zimmer, Inc.

Recalled Item: Persona Recalled by Zimmer, Inc. Due to All lots of the Persona Cemented...

The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare ADVIA Centaur Theophylline 2 (THE02) 250 Test 08838753...

The Issue: Operating range of the ADVIA Centaur systems is 18¿C to 30¿C (64.4¿F to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare BNP (8-type Natriuretic Peptide) 500 Test kit 02816634...

The Issue: Operating range of the ADVIA Centaur systems is 18¿C to 30¿C (64.4¿F to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Zimmer, Inc.

Recalled Item: Persona The Personalized Knee System Recalled by Zimmer, Inc. Due to All...

The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Zimmer, Inc.

Recalled Item: Persona Recalled by Zimmer, Inc. Due to All lots of the Persona Cemented...

The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Zimmer, Inc.

Recalled Item: Persona Recalled by Zimmer, Inc. Due to All lots of the Persona Cemented...

The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare ADVIA Centaur Folate (FOL) 500 Test 06891541 100 Recalled...

The Issue: Operating range of the ADVIA Centaur systems is 18C¿ to 30¿C (64.4¿F to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Zimmer, Inc.

Recalled Item: Persona The Personalized Knee System Recalled by Zimmer, Inc. Due to All...

The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Zimmer, Inc.

Recalled Item: Persona Recalled by Zimmer, Inc. Due to All lots of the Persona Cemented...

The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 220/240V AC Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Terumo Cardiovascular System (TCVS) has received reports of a situation...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: 100/120V AC Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Terumo Cardiovascular System (TCVS) has received reports of a situation...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Zimmer, Inc.

Recalled Item: Persona Recalled by Zimmer, Inc. Due to All lots of the Persona Cemented...

The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Zimmer, Inc.

Recalled Item: Persona Recalled by Zimmer, Inc. Due to All lots of the Persona Cemented...

The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· B Braun Medical, Inc.

Recalled Item: Outlook ES pump is intended for use with B. Braun Recalled by B Braun...

The Issue: This notice is being provided in follow up to the field correction initiated...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 14, 2012· Zimmer, Inc.

Recalled Item: Persona Recalled by Zimmer, Inc. Due to All lots of the Persona Cemented...

The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2012· Medtronic Navigation, Inc.

Recalled Item: The Vertex Max Drill Tube is a component within the Recalled by Medtronic...

The Issue: Medtronic is recalling certain Vertex Max Drill Tubes which are used with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2012· Leica Microsystems, Inc.

Recalled Item: Leica ASP6025 Vacuum Tissue Processor The Leica ASP6025 is a Recalled by...

The Issue: The Instruction for Use 1v9 and all previous versions specify incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2012· Zimmer, Inc.

Recalled Item: Zimmer Spine Ardis Inserter Recalled by Zimmer, Inc. Due to Zimmer Spine has...

The Issue: Zimmer Spine has received reports of the PEEK Ardis Interbody Spacer...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 12, 2012· Becton Dickinson & Company

Recalled Item: BD Vacutainer Buffered Sodium Citrate (9NC) Plus Blood Collection Tubes...

The Issue: BD is conducting a recall of the BD Vacutainer 2.7mL Plus Citrate Blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2012· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...

The Issue: There have been a few reported cases of the catheter breaking when removing...

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

Class II — Potential Health HazardOngoing