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. 2,622 recalls have been distributed to District of Columbia in the last 12 months.
Showing 6901–6920 of 47,654 recalls
Recalled Item: Soltive SuperPulsed Laser System TFL FIBER CLEAVER Recalled by Olympus...
The Issue: The strippers and cleavers are provided non-sterile and labelled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. CYF-V2 Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. CYF-VH Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. CYF-VHR Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. BF-XP190 Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. CYF-V2R Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. CYF-5R Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. BF-P190 Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. CYF-5 Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model No. ENF-XP Recalled by Shirakawa Olympus Co., Ltd. Due to Olympus has...
The Issue: Olympus has updated the instructions for use: Reusable cleaning brushes have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spring Valley Biotin & Collagen Liquid Recalled by BioMylz Pvt. Ltd. Due to...
The Issue: Potential mold contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Scorpio-Flex Ttl Kn P-S Tib Brg Insrt Asy- -Intended for Recalled by...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMARY REV.TIB.INSERT-DURACON Intended for knee replacement. Product...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement Recalled...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #11 -Intended for knee...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEFT SMALL-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement. Product...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3710...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #9 -Intended for knee Recalled...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #7 -Intended for knee Recalled...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3110...
The Issue: Product manufactured using UHMWPE raw material over 5 years of age has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.