State

Maryland product recalls

72,986 recalls have nationwide distribution and so reach Maryland. 8,219 additional recalls listed Maryland specifically in their distribution scope.

What the numbers show

Total: 8,219
Critical: 996
Severe: 2,132
Most recent: 2026-09-25

Of the 8,219 recalls naming Maryland we have scored against our rubric, 996 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,132 (26%) are Severe.

Which agencies issued them

These figures cover only the 8,219 recalls whose distribution notice names Maryland specifically. The 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7901–7925 of 81205

HighFDA (Drugs)·D-0276-2025·2025-03-19
Kids by babyganics mineral sunscreen recalled for chemical contamination
Kids by babyganics SPF 50 mineral sunscreen spray is being recalled due to chemical contamination. Consumers using affected batches should stop use immediately.
Product
Kids by babyganics SPF 50 mineral sunscreen totally tropical (titanium dioxide 3/5%, zinc oxide 7.25%), packaged in 3 OZ spray bottles, Dist. by KAS Direct LLC, 1525 Howe St. Racine, WI 53403, UPC 813277019923 and UPC 813277019916
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0270-2025·2025-03-19
Duloxetine 30mg Delayed-Release Capsules Recalled for N-Nitroso Impurity
Breckenridge Pharmaceutical recalls 14,749 bottles of duloxetine 30mg delayed-release capsules due to N-nitroso impurity above FDA safety limits. Patients taking this medication should contact their healthcare provider to verify if their prescription is affected.
Product
DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0634-2025·2025-03-19
Ulker Dankek Roll Cake Chocolate recalled due to undeclared egg allergen
Ulker Dankek Roll Cake Chocolate is being recalled because egg is not listed in the Contains statement on the product label. Consumers with egg allergies may be at risk.
Product
Ulker Dankek Roll Cake Chocolate, item 9584, 3oz foil pack, 8 per case, UPC 8690504067979
Category
Food
Distribution
36 states
HighFDA (Devices)·Z-1313-2025·2025-03-19
TruScan Body dental scanner recalled due to scanning malfunction
TruAbutment Inc. recalls 61 units of the TruScan Body dental scanner (CN38-SB) due to defects that may prevent proper or accurate scanning.
Product
Brand Name: TruScan Body, REF CN38-SB Product Name: TruScan Body compatible with CONELOG 3.8 Model/Catalog Number: CN38-SB Software Version: N/A
Category
Medical Device
Distribution
16 states
HighFDA (Drugs)·D-0271-2025·2025-03-19
Duloxetine Capsules Recalled for N-Nitroso Impurity Exceeding FDA Limits
Breckenridge Pharmaceutical is recalling 11,125 bottles of Duloxetine 20mg capsules nationwide due to N-nitroso-duloxetine impurity above FDA-recommended limits. The impurity was detected during quality control testing.
Product
DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1322-2025·2025-03-19
ZOLL Powerheart G5 AED Self-Test May Fail Under Extreme Environmental Conditions
ZOLL is recalling certain Powerheart G5 AED units that may fail their self-test when exposed to extreme temperatures or humidity. The affected devices could fail to function properly in emergencies.
Product
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5S-00A-TSO, (2) G5S-01A, (3) G5S-02A, (4) G5S-05A, (5) G5S-08A, (6) G5S-10A, (7) G5S-11A, (8) G5S-80A-TSO, (9) G5S-80-L (10) G5S-90A; Software Version: NA Product Description: The Powerheart G5 automa
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0619-2025·2025-03-19
Van Camp's Canned Tuna Recalled for Potential Botulism Risk from Faulty Lids
Chicken of the Sea is recalling 14,147 cases of Van Camp's Solid Light Yellowfin Tuna due to improperly secured easy-pull lids that may allow Clostridium botulinum contamination. No illnesses have been reported.
Product
Van Camp's branded Solid Light Yellowfin in Vegetable oil; NET WT. 5 OZ (142g) DR WT. 4 OZ (113g); Distributed by: Chicken of The Sea Intl.; El Segundo, CA 90245 U.S.A. UPC# 48000 25015 UPC# 48000 75015
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1315-2025·2025-03-19
Cartilage Transplant System Disposable Kits Recalled for Missing Component
DePuy Mitek is recalling COR Disposable Kit cartilage transplant systems because some units lack the pin in the graft loader component. The manufacturing defect may prevent proper device function during surgical use.
Product
COR Disposable Kit, 8 mm w/ Perpendicularity. Cartilage Transplant System.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V172000·2025-03-19
Tesla Model S and X may have an inoperative horn
Tesla is recalling certain 2021-2024 Model S and 2021-2025 Model X vehicles because an airbag with the incorrect horn pad may have been installed, preventing the horn from sounding.
Product
TESLA — TESLA MODEL S, MODEL X
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0274-2025·2025-03-19
Walgreens Acne Control Cleanser recalled for benzene contamination
Walgreens Acne Control Cleanser with 10% benzoyl peroxide is being recalled nationwide due to benzene contamination. The affected lot (23-09328, exp. 09/2025) was distributed across the U.S.
Product
Walgreens, Acne Control Cleanser, 10% Benzoyl Peroxide/Acne Treatment, NET WT 5 OZ (142g) Distributed by: Walgreen CO, 200 Wilmont RD, Deerfield, IL, Made in Canada. UPC#: 1 9560203602 8
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0626-2025·2025-03-19
Danone Hazelnut Delight Coffee Creamer Recalled for Spoilage and Illness
Danone is recalling Hazelnut International Delight Coffee Creamer due to reported spoilage and illness complaints. The product was distributed to 30 states.
Product
HAZELNUT INTERNATIONAL delight COFFEE CREAMER 32 FL OZ (1 QT) 32 FL OZ (1 QT) 946 mL UPC 0 41271 02565 2 Distributed by: Danone US, LLC
Category
Food
Distribution
31 states
HighFDA (Food)·F-0615-2025·2025-03-19
Trader Joe's Canned Albacore Tuna Recalled for Potential Botulism Contamination
Trader Joe's Solid White Albacore Tuna is being recalled because the easy-pull lid may not be properly secured, risking contamination with botulism bacteria.
Product
Trader Joe's branded Solid White Albacore Tuna in olive oil; NET WT. 5 OZ (142g) DR WT. 4 OZ (113g); Dist & Sold Exclusively By: Trader Joe's, Monrovia, CA 91816; UPC# 99287
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0612-2025·2025-03-19
Trader Joe's Solid White Albacore Tuna Recalled for Defective Lid
Trader Joe's Solid White Albacore Tuna (5 oz cans) is being recalled due to improperly secured lids that may allow contamination with Clostridium botulinum. Affected products have Best By dates of 01/08/2028 or 01/09/2028.
Product
Trader Joe's branded Solid White Albacore Tuna in Water, no salt added; NET WT. 5 OZ (142g) DR WT. 4 OZ (113g); Dist & Sold Exclusively By: Trader Joe's, Monrovia, CA 91816; UPC# 0099 2848
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1307-2025·2025-03-19
CardiFocus Heartlight X3 Cardiac Catheter Sterile Barrier Damage Recall
CardioFocus is recalling 833 units of CardiFocus Heartlight X3 cardiac catheters due to potential damage to the sterile barrier pouch that could compromise product sterility. Affected units were distributed worldwide.
Product
CardiFocus Heartlight X3 Catheter- Intended in the treatment of atrial fibrillation. It is introduced percutaneously in the setting of an Electrophysiology or Catheterization Laboratory Model: 18-5000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0635-2025·2025-03-19
Ulker Dankek Roll Cake Banana recalled for undeclared wheat allergen
ZB Importing LLC is recalling Ulker Dankek Roll Cake Banana due to wheat allergen not being listed in the product label. Consumers with wheat allergies or celiac disease should not consume this product.
Product
Ulker Dankek Roll Cake Banana, item 9620, 8.3oz foil pack, 8 per case, UPC 8690504067986
Category
Food
Distribution
36 states
HighFDA (Drugs)·D-0269-2025·2025-03-19
Duloxetine 60mg Capsule Recall Due to Manufacturing Impurity
Breckenridge Pharmaceutical recalls 11,100 bottles of Duloxetine 60mg capsules distributed nationwide due to the presence of N-nitroso-duloxetine impurity exceeding FDA recommended interim limits from manufacturing deviations.
Product
DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1316-2025·2025-03-19
ZOLL Powerheart G5 AED May Fail Self-Test in Extreme Conditions
The ZOLL Powerheart G5 automated external defibrillator may fail its self-test after prolonged exposure to extreme temperatures or humidity levels. This could prevent proper device functioning in an emergency.
Product
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-00A, (2) G5A-01A, (3) G5A-02A, (4) G5A-03A, (5) G5A-19A, (6) G5A-80A, (7) G5A-80A-TSO. Software Version: NA Product Description: The Powerheart G5 automated external defibrillator (AED) is designed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1312-2025·2025-03-19
Aesculap hemostatic forceps recalled due to clamp breakage
Aesculap is recalling 47,078 surgical forceps designed to control bleeding. The devices' clamps break when used outside design parameters, potentially compromising their effectiveness.
Product
Numerous models of nonsterile hemostatic forceps: (1) REF BH951R, Negus Tonsil Forceps HVY-CVD 190MM; (2) REF BH952R, Negus Tonsil Forceps X-HVY-CVD190MM; (3) REF BH957R, Schnidt Tonsil Forceps SLT-CVD185MM; (4) REF BH959R, Schnidt Tonsil Forceps CVD 185MM; (5) REF BH961R,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1323-2025·2025-03-19
ZOLL Powerheart G5 AED Devices Recalled for Self-Test Failure Risk
ZOLL is recalling 8,744 Powerheart G5 AED units that may fail their self-test if exposed to extreme temperatures or humidity, potentially masking device malfunctions.
Product
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: G5S-80A; Software Version: NA Product Description: The Powerheart G5 automated external defibrillator (AED) is designed for treating life-threatening heart beat irregularities, such as ventricular fibrilla
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1326-2025·2025-03-19
Beckman Coulter DxI 9000 Analyzer wash wheel mixer defect may prevent operation
Beckman Coulter is recalling the DxI 9000 Access Immunoassay Analyzer due to a mechanical defect in the wash wheel mixer that may prevent the device from operating properly. The defect can cause test delays or cancellation.
Product
DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0632-2025·2025-03-19
Ulker Dankek Roll Cake Strawberry recalled due to undeclared milk allergen
ZB Importing LLC is recalling Ulker Dankek Roll Cake Strawberry because milk is not declared on the label. Products were distributed in multiple US states and Ontario, Canada.
Product
Ulker Dankek Roll Cake Strawberry , item 8298, 8.3oz foil pack, 8 per case, UPC 8690504066828
Category
Food
Distribution
36 states
HighFDA (Drugs)·D-0273-2025·2025-03-19
Acne treatment gel recalled for benzene contamination nationwide
Zapzyt Acne Treatment Gel (10% benzoyl peroxide) distributed nationwide is being recalled due to contamination with benzene. Consumers should stop using affected lots immediately.
Product
ZAPZYT ACNE TREATMENT GEL — ZAPZYT ACNE TREATMENT GEL (BENZOYL PEROXIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0611-2025·2025-03-19
Genova Yellowfin Tuna Cans Recalled for Botulism Risk
Genova branded Yellowfin Tuna cans are being recalled because the easy-pull lid was not properly secured, which may cause Clostridium botulinum contamination. The recall affects 14,147 cases distributed nationwide with best-by dates from December 2027 through January 2028.
Product
Genova branded Yellowfin Tuna; Genova; In Olive Oil; Wild Caught; NET WT. 5 OZ (142g) RD WT. 4 OZ (113g); Distributed by Tri-Union Seafoods, LLC.; El Sugundo, CA 90245 U.S.A. UPC# 48000 73265 UPC# 48000 13265 UPC# 48000 63267 Product is packaged in several different configurat
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0613-2025·2025-03-19
Trader Joe's Tuna Recall Due to Unsealed Lids, Botulism Risk
Trader Joe's Solid White Albacore Tuna in Water is being recalled because improperly secured easy-pull lids may allow contamination with Clostridium botulinum.
Product
Trader Joe's branded Solid White Albacore Tuna in Water, salt added; NET WT. 5 OZ (142g) DR WT. 4 OZ (113g); Dist & Sold Exclusively By: Trader Joe's, Monrovia, CA 91816; UPC# 0099285
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1321-2025·2025-03-19
ZOLL Powerheart G5 AED devices may fail self-test in extreme environments
ZOLL is recalling Powerheart G5 AED devices that may fail their self-test when exposed to extreme temperature or humidity, potentially affecting proper device operation.
Product
Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: G5S-80C; Software Version: NA Product Description: The Powerheart G5 automated external defibrillator (AED) is designed for treating life-threatening heart beat irregularities, such as ventricular fibrilla
Category
Medical Device
Distribution
Distributed nationwide