State

District of Columbia product recalls

73,576 recalls have nationwide distribution and so reach DC. 2,798 additional recalls listed District of Columbia specifically in their distribution scope.

What the numbers show

Total: 2,798
Critical: 240
Severe: 1,083
Most recent: 2026-09-23

Of the 2,798 recalls naming District of Columbia we have scored against our rubric, 240 (9%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,083 (39%) are Severe.

Which agencies issued them

These figures cover only the 2,798 recalls whose distribution notice names District of Columbia specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25576–25600 of 76374

SevereFDA (Drugs)·D-0633-2021·2021-06-30
PremierZEN Gold 7000 Capsule Recalled for Undisclosed Drug Contamination
PremierZEN Gold 7000 capsules are recalled nationwide because the product contains undisclosed pharmaceutical ingredients Sildenafil and Tadalafil and was marketed without FDA approval.
Product
PremierZEN Gold 7000 capsule, 1-count blister card, packaged in 12 cards per box (UPC 7 28175 42183 2), Distributed by: New Premier Group, Los Angeles, CA 90006
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0635-2021·2021-06-30
maXXzen Platinum 12000 Capsule Recalled for Undisclosed Drug Contaminants
The FDA is recalling maXXzen Platinum 12000 capsules distributed nationwide because the product was marketed without an approved application and contains undisclosed pharmaceutical ingredients (Sildenafil and Tadalafil).
Product
maXXzen Platinum 12000 capsule, 1-count blister card (UPC 7 18122 04072 8), Distributed by: Maxx Inc, Los Angeles, CA 90028
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1863-2021·2021-06-30
Nitric Oxide Delivery System Dosing Deficiency During Console Transitions
GENOSYL DS Nitric Oxide Delivery System is recalled for delivering below-intended doses during transitions between primary and backup consoles following a software update.
Product
GENOSYL DS; Nitric Oxide Delivery System Combination Product NDA202860
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0688-2021·2021-06-30
Clio Coconut Yogurt Bars Recalled for Possible Metal Fragments
Clio LLC is recalling Clio Coconut Less Sugar Yogurt Bars (45g and 50g 10-packs) distributed nationwide due to possible metal fragments in the product.
Product
Clio Coconut Less Sugar Yogurt Bars wrapped in a Chocolate Coating 45g x 10 Clio Retail 10-pack and 50g x 10 Clio Retail 10-pack, UPC codes: 854021008237 and 854021008046
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1934-2021·2021-06-30
Dexcom G6 Sensor 3-Pack Recalled for Temperature-Related Measurement Errors
Cardinal Health is recalling 2,357 kits of Dexcom G6 Sensor 3-Pack due to temperature exposure during shipping that may cause inaccurate glucose readings. Affected units were distributed in Florida, Georgia, and South Carolina.
Product
DEXCOM G6 SENSOR 3 PACK Item Number: 5447552
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1930-2021·2021-06-30
FREESTYLE LIBRE 14 DAY glucose monitoring system recalled for temperature exposure
Cardinal Health is recalling 8,959 glucose monitoring kits due to temperature exposure during shipping that may result in inaccurate readings. Affected devices were distributed nationwide.
Product
FREESTYLE LIBRE 14 DAY GLUCOSE MONITORING SYSTEM. Item Number: 5479084
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1931-2021·2021-06-30
FreeStyle Libre 2 Glucose Monitoring System Recalled for Inaccurate Results
Cardinal Health is recalling FreeStyle Libre 2 glucose monitoring systems shipped between February and March 2021 due to temperature exposure during shipment that may cause inaccurate readings.
Product
FREESTYLE LIBRE 2 GLUCOSE MONITORING SYSTEM: Item number: 5658877
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0694-2021·2021-06-30
Clio Peanut Butter Greek Yogurt Bars Recalled for Possible Metal Fragments
Clio LLC is recalling Peanut Butter Greek Yogurt Bars due to the possible presence of metal fragments. The affected product was distributed nationwide with best-buy dates between March 7, 2021 and June 20, 2021.
Product
Clio Peanut Butter Greek Yogurt Bars wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack, UPC code: 854021008039
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1944-2021·2021-06-30
FilmArray Pneumonia Panel diagnostic test kits recalled for false results
BioFire Diagnostics is recalling 9 FilmArray Pneumonia Panel test kits due to manufacturing defects causing false positive and negative test results, as well as control failures.
Product
FilmArray Pneumonia Panel (Penumo) REF RFIT-ASY-0144
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21156·2021-06-30
Children's Nightgowns Recalled for Flammability Standard Violation
Auranso Official children's nightgowns sold on Amazon fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries. About 8,000 units distributed January–June 2021 are affected.
Product
Children's Nightgowns
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1939-2021·2021-06-30
OneTouch Delica Lancets Recalled Due to Temperature Exposure During Shipping
Cardinal Health is recalling OneTouch Delica Lancets (100-count boxes) after devices were exposed to freezing temperatures during shipping, which may affect blood glucose test accuracy. No injuries have been reported.
Product
ONETOUCH DELICA LANCETS 30G 100 COUNT Item Number: 5541610
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0687-2021·2021-06-30
Clio Coconut Greek Yogurt Bars recalled for possible metal fragments
Clio LLC is recalling Clio Coconut Greek Yogurt Bars in 50g x 10-pack format due to the possible presence of metal fragments. The product was distributed nationwide.
Product
Clio Coconut Greek Yogurt Bars wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack, UPC: 854021008046
Category
Food
Distribution
Distributed nationwide
HighCPSC·21159·2021-06-30
Children's Robes Fail Federal Flammability Standards, Pose Burn Risk
SIORO-branded children's robes sold on Amazon from December 2020 through April 2021 fail to meet federal flammability standards for sleepwear, posing a risk of burn injuries to children.
Product
Children's Robes
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-0685-2021·2021-06-30
Clio Strawberry Greek Yogurt Mini Bars Recalled for Possible Metal Fragments
Clio LLC is recalling Clio Strawberry Greek Yogurt Mini Bars (6.2 oz pouch x 6 pouches per case, UPC 854021008084) with best buy dates between 2/7/2021 and 6/27/2021 due to possible metal fragments.
Product
Clio Strawberry Greek Yogurt Mini Bars wrapped in a Chocolate Coating 6.2oz pouch x 6 pouches per case, UPC: 854021008084
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0703-2021·2021-06-30
Favorite Day Peanut Butter Monster Trail Mix Recall for Plastic Contamination
John B. Sanfilippo & Son Inc. is recalling Favorite Day Peanut Butter Monster Trail Mix because the product may contain stringy pieces of flexible plastic. The affected product was distributed nationwide.
Product
favorite day peanut butter monster Trail Mix, Product Number 04316. Peanuts, peanut butter chips, raisins, M&M'S peanut butter chocolate candies, peanut butter pretzel balls, and mini peanut butter cups. Net Wt 14 oz. (396g), UPC 85239-15684
Category
Food
Distribution
Distributed nationwide
HighCPSC·21158·2021-06-30
UPPAbaby RumbleSeat Adapters Recalled for Child Fall Hazard
UPPAbaby is recalling approximately 86,000 RumbleSeat adapters that can detach from strollers, posing a fall hazard to children. The company has received 135 reports of detachments, including injuries such as bumps, scrapes, and two broken noses.
Product
UPPAbaby adapters included with Rumbleseats
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-0691-2021·2021-06-30
Clio Mixed Berry/Peach Greek Yogurt Bars Recalled for Possible Metal Fragments
Clio LLC is recalling Clio Mixed Berry/Peach Greek Yogurt Bars sold at Costco due to possible metal fragments in the product. Consumers should not consume the affected items.
Product
Clio Mixed Berry / Peach Greek Yogurt Bars wrapped in a Chocolate Coating Costco Club pack Clio 50g x 16 (12pc tray), UPC code: 854021008220
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1946-2021·2021-06-30
Medical Action Curved Hemostats recalled due to flaking metal risk
Medical Action Industries is recalling curved hemostats distributed across 16 U.S. states due to a manufacturing defect causing potential metal flaking and discoloration.
Product
Medical Action INDUSTRIES INC., Disposable Instrument Pack Curved Hemostat, REF 56224
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0695-2021·2021-06-30
Clio Yogurt Bars Recalled for Possible Metal Fragments
Clio LLC is recalling Raspberry/Peach Sams Mini Club Yogurt Bars due to the possible presence of metal fragments. The recalled product was distributed nationwide.
Product
Clio Raspberry / Peach Sams Mini Club Yogurt Bars wrapped in a Chocolate Coating 24g x 24 (12pc tray), UPC code: 854021008251
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1903-2021·2021-06-30
Blood Culture Identification Panel Recalled Due to Manufacturing Defect
BioFire BCID2 panels for FilmArray Systems are recalled due to manufacturing defects causing elevated rates of false negative results. Affected diagnostic kits may fail to detect infections in blood culture samples.
Product
BioFire BCID2 Panel, REF RFIT-ASY-0147, For FilmArray Systems, CE, Blood Culture Identification Panel in vitro diagnostic, Rx Only, UDI: (01)00815381020338
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1902-2021·2021-06-30
Ventec VOCSN Ventilators May Shut Down Due to Component Failure
Ventec VOCSN ventilators may unexpectedly shut down or lose blower function during patient use due to component failure. This could prevent the device from providing ventilation therapy. About 1,934 devices are affected.
Product
Ventec Life Systems VOCSN Multi-Function Ventilator Model/Version/Catalog Number: V+O+C+S+N+Pro/English/PRT-00490-001; V+O+C+S+N+Pro/Japan/PRT-00490-100; V+C+Pro/English/PRT-00900-001; V+C+Pro/Japan/PRT-00900-100; V+C/English/PRT-01098-000…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1938-2021·2021-06-30
OneTouch Ultra Test Strips Recalled for Potential Inaccurate Glucose Readings
Cardinal Health Inc. is recalling OneTouch Ultra Test Strips (item 3510443) because temperature excursions during shipping may have compromised glucose measurement accuracy.
Product
ONETOUCH ULTRA TEST STRIPS 25 COUNT Item Number: 3510443
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1933-2021·2021-06-30
Prefilled Pen Needles Recalled Due to Temperature Exposure During Shipping
Cardinal Health is recalling 1,599 boxes of prefilled pen needles that were exposed to low temperatures during shipping, which may cause inaccurate results. Affected units were distributed in Florida, Georgia, and South Carolina.
Product
BD UF PEN 32GX4MM 100 NANO Item Number: 4292272
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0684-2021·2021-06-30
Clio Greek Yogurt Bars Recalled for Possible Metal Fragments
Clio LLC is recalling Clio Greek Yogurt Bars (50g x 10 retail packs) distributed nationwide due to the possibility of metal fragments in the product.
Product
Clio Greek Yogurt Bar wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack, UPC: 867155000206
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1949-2021·2021-06-30
FDA Recalls Medical Action Minor Procedure Trays for Flaking Metal on Hemostats
Medical Action Industries is recalling 31 cases of Minor Procedure Trays because hemostats in the kits may have flaking metal or brown spots that could compromise sterile surgical procedures.
Product
Medical Action INDUSTRIES INC., Minor Procedure Tray, REF 61214
Category
Medical Device
Distribution
Distributed nationwide