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. 2,495 recalls have been distributed to Delaware in the last 12 months.

48,330 total recalls
2,495 in last 12 months

Showing 2108121100 of 27,373 recalls

Medical DeviceJune 30, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software anomaly may...

The Issue: Software anomaly may occur during the installation of an Assay Data Diskette...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Processor EPX 2500 High Definition Endoscopy Recalled by Fujifilm...

The Issue: The EPX-2500 Operation Manual and sales brochure incorrectly identify that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Covidien LP (formerly Nellcor Puritan Bennett Inc.)

Recalled Item: OxiMax N-560 Pulse Oximeter. For continuous or spot check monitoring...

The Issue: Potential missing segments on the display that can result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Merit Medical Systems, Inc.

Recalled Item: ReSolve Locking Drainage Catheters The ReSolve Locking Catheters are...

The Issue: Merit Medical Systems, Inc. is voluntarily conducting a recall due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Baxter Healthcare Corp.

Recalled Item: Baxter HomeChoice and HomeChoice Pro APD systems Recalled by Baxter...

The Issue: Loud operating sounds, which was unacceptable to the end users when the...

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

Class III — Low RiskOngoing
Medical DeviceJune 29, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis zee systems Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: The possibility exists for a large amount of liquid to seep through the top...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Axiom Artis systems Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: The possibility exists for a large amount of liquid to seep through the top...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Becton Dickinson & Co.

Recalled Item: Enterococcus Screen Agar QUAD Plate Recalled by Becton Dickinson & Co. Due...

The Issue: The affected expired lots of product may have exhibited breakthrough growth...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON S Family ultrasound systems utilizing the 18L6 HD and/or Recalled by...

The Issue: When using the CIVCO biopsy attachments in combination with the ACUSON S...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Becton Dickinson & Co.

Recalled Item: Vancomycin Screen Agar Recalled by Becton Dickinson & Co. Due to The...

The Issue: The affected expired lots of product may have exhibited breakthrough growth...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q systems Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The possibility exists for a large amount of liquid to seep through the top...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2015· Covidien LP (formerly Nellcor Puritan Bennett Inc.)

Recalled Item: OxiMax N-65 Handheld Pulse Oximeter. N65 Recalled by Covidien LP (formerly...

The Issue: Potential missing segments on the display that can result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics MDR Acinetobacter container type: 15x100mm monoplate...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics MacConkey Agar with CiPRP Recalled by Hardy Diagnostics...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics BHI with CIPRO Recalled by Hardy Diagnostics Due to Hardy...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics BEA Agar with VGA container type: 15x100mm monoplate...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics BEA Agar with Vancomycin container type: 15x100mm...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Hardy Diagnostics

Recalled Item: Hardy Diagnostics BEA Broth with Vancomycin container type: 13x100mm tube...

The Issue: Hardy Diagnostics is recalling MacConkey Agar with Ciprofloxacin, Brain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Siemens Medical Solutions USA, Inc.

Recalled Item: e.cam Gamma Camera Recalled by Siemens Medical Solutions USA, Inc. Due to...

The Issue: Potential failure mode related to the radial brake, where the detector was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2015· Alere Scarborough, Inc. dba Binax, Inc.

Recalled Item: Alere i flu Recalled by Alere Scarborough, Inc. dba Binax, Inc. Due to Risk...

The Issue: Risk of false negative results due to microbial growth in the Sample...

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

Class II — Potential Health HazardOngoing