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. 2,582 recalls have been distributed to Delaware in the last 12 months.
Showing 14721–14740 of 27,373 recalls
Recalled Item: APTIO RACK OUTPUT MODULE Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portable Suction Pump Recalled by Ohio Medical Corporation Due to The...
The Issue: The care-e-vac(R)3 Battery/AC Powered Portable Aspirator battery terminal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLAB - STORAGE MODULE 15000 Recalled by Siemens Healthcare Diagnostics,...
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTIO 15000 STORAGE MODULE Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IsoFlex LAL Support Surface Recalled by Stryker Medical Division of Stryker...
The Issue: Certain 2860 IsoFlex LAL support surfaces were assembled with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVS Aria Cage Recalled by Stryker Spine Due to The anterior and posterior...
The Issue: The anterior and posterior markers on the cage were on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK(R) 2 AST-P655 Recalled by bioMerieux, Inc. Due to Routine internal...
The Issue: Routine internal review of Device History Records identified six VITEK(R) 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK(R) 2 AST-P640 Recalled by bioMerieux, Inc. Due to Routine internal...
The Issue: Routine internal review of Device History Records identified six VITEK(R) 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VaccZyme Human Anti-Haemophilus influenza type b Enzyme Immunoassay Kit For...
The Issue: A deterioration of performance was identified with influenza type B Enzyme...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pointe Scientific AutoHDL/LDL Cholesterol Calibrator Recalled by Medtest...
The Issue: Vials of the autoHDL/LDL Calibrator were shipped without a vial label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ambu Aura40 Standard Recalled by Besmed Health Business Corporation Due to...
The Issue: Ambu Aura40 Standard, Reusable Laryngeal Mask packaged in a pouch marked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Recalled...
The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HipLOC Hip Fracture Fixation System-Hiploc System 140¿ Plate 38 mm Recalled...
The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Recalled...
The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HipLOC Hip Fracture Fixation System- Hiploc System 130¿ Plate 38 Recalled by...
The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchofiberscope BF-40 Recalled by Olympus Corporation of the Americas Due...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Right 125 13 mm x 300 mm Recalled by Zimmer...
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail 125 9 mm x 165 mm Recalled by Zimmer Biomet, Inc....
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Left 125 9 mm x 320 mm Recalled by Zimmer Biomet,...
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Right 125 13 mm x 360 mm Recalled by Zimmer...
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.