Product Recalls in District of Columbia
Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,629 recalls have been distributed to District of Columbia in the last 12 months.
Showing 5761–5780 of 27,451 recalls
Recalled Item: SurgiCount+ Software Application-indicated as an adjunctive technology for...
The Issue: Potential for current software to miscount when scanning in multiple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH LDL Cholesterol- In vitro diagnostic use in the Recalled by...
The Issue: Potential for reagent carryover on the Atellica CH 930 resulting in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Five S 5 3x65 Recalled by Karl Storz Endoscopy Due to Flexible intubation...
The Issue: Flexible intubation endoscopes sterility assurance can not be confirmed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIF AMP Recalled by Alphatec Spine, Inc. Due to Awl instrument adjustable...
The Issue: Awl instrument adjustable drill button assembly assembled in the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APK2 Pressure-Sensing Wheelchair Cushions Recalled by Aquila Corporation Due...
The Issue: Defective battery pack in wheelchair cushions can overheat resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SofTech Pressure-Sensing Wheelchair Cushions Recalled by Aquila Corporation...
The Issue: Defective battery pack in wheelchair cushions can overheat resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...
The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...
The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...
The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Hip Kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to The...
The Issue: The prep solution included in the Total Hip Kit expires prior to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...
The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...
The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...
The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...
The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...
The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...
The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...
The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...
The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...
The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3D9-3v Transducer Recalled by Philips Ultrasound, Inc. Due to Transducer, an...
The Issue: Transducer, an ultrasound system accessory, consists of two parts that are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.