Product Recalls in Maryland
Product recalls affecting Maryland — including food, drugs, consumer products, medical devices, and vehicles distributed to Maryland. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,877 recalls have been distributed to Maryland in the last 12 months.
Showing 4621–4640 of 29,093 recalls
Recalled Item: TRIDENTII PSL CLUSTER52E- Indicated for use in primary and revision Recalled...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII HEMI CLUSTER48D-indicated for use in primary and revision patients...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz SE & CO. KG Recalled by Karl Storz Endoscopy Due to Inadequate...
The Issue: Inadequate reprocessing validation evidence
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII HEMI CLUSTER66H- Indicated for use in primary and revision...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII PSL CLUSTER48D- Indicated for use in primary and revision Recalled...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII PSL CLUSTER58F-Indicated for use in primary and revision patients...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII HEMI CLUSTER54E- Indicated for use in primary and revision...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz SE & CO. KG Recalled by Karl Storz Endoscopy Due to Inadequate...
The Issue: Inadequate reprocessing validation evidence
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII PSL CLUSTER50D- Indicated for use in primary and revision Recalled...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII PSL CLUSTER64H- Indicated for use in primary and revision Recalled...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaviNetics Skull Anchor Key and Drill Kit Recalled by Navinetics Inc Due to...
The Issue: Defective Skull Anchor Key. After attachment of the single use Skull Anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Pressure Unit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: The firm provided a set of specifications for the device, but some units of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Sub-G Endotracheal Tube with Subglottic Suctioning: (1) Recalled by...
The Issue: Complaints have been received that the device inflation tube detached and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation Auxiliary ES . Intended to securely Recalled by...
The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation ES (Med ES Main) . Intended Recalled by CareFusion 303,...
The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation Auxiliary 4000 . Intended to securely Recalled by...
The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LeadCare¿ II Blood Lead Test System relies on electrochemistry Recalled...
The Issue: Calibration Buttons being used in the kitting process were incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation 4000 . Intended to securely store Recalled by CareFusion...
The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE M1S0179 STRL TAPE/PEN PACK Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Product may have a weak seal which may result in a breach of sterility of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE SWABSTICKS ALCOHOL 3PK Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Product may have a weak seal which may result in a breach of sterility of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.