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.
Showing 21161–21180 of 27,373 recalls
Recalled Item: Offset Femoral Alignment Guide Recalled by Omnilife Science Inc. Due to The...
The Issue: The markings on both versions of the OFFSET FEMORAL ALIGNMENT GUIDES are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cochlear Nucleus Sterile Silicone Template Product Usage: The Cochlear ...
The Issue: Cochlear Americas is recalling Nucleus Sterile Silicone Template...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor Product Usage: The HeartStart...
The Issue: Multiple software and hardware issues with device that can affect its function.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panoramic X-ray Model PC-1000 The PC-1000 will enable the user Recalled by...
The Issue: Jackscrew nut part failure potentially leading to device malfunction and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano PV .035 Catheter: Part number: 88901 Recalled by Volcano Corporation...
The Issue: During a relabeling procedure at the manufacturing facility, the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APEX INTERFACE Hemi 54X and Flared 56X Recalled by Omnilife Science Inc. Due...
The Issue: The device may have improper screw hole placement due to inaccurate location...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prestige Plus 185cm J-Tip: Part number: 9185J Recalled by Volcano...
The Issue: During a relabeling procedure at the manufacturing facility, the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Emotion 6 Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A potential safety issue involving two (2) broken screws and one (1) bowed,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Emotion 16 Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A potential safety issue involving two (2) broken screws and one (1) bowed,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 5-detector Recalled by Perkinelmer Due to Error in...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SERFAS 90 degree Energy Probe Recalled by Stryker Endoscopy Due to Stryker...
The Issue: Stryker Endoscopy is recalling all non expired SERFAS 90 degree Energy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Femoral Drill Guide Lateral IM Adapter Product Usage: Drill Recalled...
The Issue: Oxford Femoral Drill Guide Lateral IM Adapter may have an undersized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apex ARC Hip Stem Recalled by Omnilife Science Inc. Due to Product may...
The Issue: Product may breach the inner and outer sterile pouches during shipping or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WIZARD2 5-detector Recalled by Perkinelmer Due to Error in WIZARD2 Barcode...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WIZARD2 2-detector Recalled by Perkinelmer Due to Error in WIZARD2 Barcode...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to Error in...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to Error in...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING FEMORAL HEAD Recalled by...
The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING ACETABULAR CUP W/IMPACTOR...
The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING DYSPLASIA CUP W/IMPACTOR...
The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.