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.
Showing 25921–25940 of 27,373 recalls
Recalled Item: SOL SYS 8IN CALC 1.5/18.0 Packaging: Product is packed within Recalled by...
The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOL SYS L 9IN CALC 2.25/15.0 Packaging: Product is packed Recalled by DePuy...
The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOL SYS R 9IN CALC 2.25/22.5 Packaging: Product is packed Recalled by DePuy...
The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOL SYS F 9 CALC L 13.5MM LG Packaging: Product Recalled by DePuy...
The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eon and Eon Mini charging system Recalled by St. Jude Medical Due to There...
The Issue: There is issues of warmth or heating at the implant site during charging for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Set Screw 5.5 mm Rod - Model #7703-1600. Product Usage: Recalled by Biomet...
The Issue: Biomet Spine LLC is recalling the Set Screw 5.5 mm Rod due to the set screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CO2 Incubators (General Purpose Incubator) Recalled by Thermo Fisher...
The Issue: Incubators manufactured prior to mid 2009 have coated metal hinges that have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Handset component of the Handicare USA's Minivator Bath Bliss Reclining...
The Issue: Firm became aware that two handsets in the affected batches became...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter AU5800 Clinical Chemistry Analyzer. An automated chemistry...
The Issue: Due to a software data storage limitation which only occurs under certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle Cancellous Screw Packaging: Product is housed within a polyurethane...
The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary recall of ten lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray DS USA Recalled by Mindray DS USA, Inc. d.b.a. Mindray North America...
The Issue: Mindray has identified a software anomaly that may where, in the presence of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile Diagnostic X-Ray System with Digital Panel Recalled by Philips...
The Issue: When the operator moves an image to another view then the electronic marker...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Somatom CTs equipped with software syngo CT2010A Recalled by Siemens...
The Issue: Sporadic hang-up malfunctions concerning 3D reconstructions during activated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TCM4 series Base Units Recalled by Radiometer America Inc Due to RADIOMETER...
The Issue: RADIOMETER became aware that the TCM4 series Base Unit does not comply with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...
The Issue: GranuFlo Dry Acid Concentrate may show discoloration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEOGRAM AMINO ACIDS AND ACYLCARNITINES TANDEM MASS SPECTROMETRY KIT Product...
The Issue: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...
The Issue: GranuFlo Dry Acid Concentrate may show discoloration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEONATAL TOTAL GALACTOSE KIT Product Numbers: 3029-0010 Recalled by...
The Issue: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius GranuFlo Dry Acid Concentrate For Bicarbonate Dialysis 2.0 K...
The Issue: GranuFlo Dry Acid Concentrate may show discoloration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius GranuFlo Naturalyte Dry Acid Concentrate For Bicarbonate Dialysis...
The Issue: GranuFlo Dry Acid Concentrate may show discoloration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.