State

Maryland product recalls

73,566 recalls have nationwide distribution and so reach Maryland. 8,225 additional recalls listed Maryland specifically in their distribution scope.

What the numbers show

Total: 8,225
Critical: 996
Severe: 2,516
Most recent: 2026-10-21

Of the 8,225 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 2,516 (31%) are Severe.

Which agencies issued them

These figures cover only the 8,225 recalls whose distribution notice names Maryland specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25776–25800 of 81791

HighFDA (Food)·F-0033-2022·2021-10-27
Chocolate & the Chip Cookies Recalled for Undeclared Allergens
Chocolate & the Chip is recalling Fluffadoodle and Fluffa-Nutta Cookies due to undeclared wheat, milk, and soy allergens found on packaging labels during a California health inspection.
Product
Chocolate & the Chip Fluffadoodle and Fluffa-Nutta Cookies: 4 oz / 114 grams per pack. Cookies are packaged in uniform pairs in a food grade clear resealable bag and label Corrected Ingredients: Ingredients: All purpose flour (bleached wheat flour, malted barley flour…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0135-2022·2021-10-27
Discovery MR750w 3.0T MRI: Missing Image Slices in 3D Volume
GE Healthcare recalls the Discovery MR750w 3.0T MRI system. Under certain software conditions, image slices may be missing, creating gaps in 3D diagnostic images.
Product
Discovery MR750w 3.0T nuclear magnetic resonance imaging system
Category
Medical Device
Distribution
19 states
HighFDA (Food)·F-0036-2022·2021-10-27
Chocolate & the Chip Octoberfest Cookies Recalled for Undeclared Allergens
Chocolate & the Chip Octoberfest Cookies are being recalled due to undeclared wheat, milk, and soy allergens found on product labels during a California Department of Public Health inspection.
Product
Chocolate & the Chip Octoberfest Cookies: 4 oz / 114 grams per pack. Cookies are packaged in uniform pairs in a food grade clear resealable bag and label Corrected Ingredients: Not provided. Labels found during the inspection had undeclared wheat, milk, soy. Firm had listed…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0042-2022·2021-10-27
Chocolate & the Chip Lavender Cookies Recalled for Undeclared Allergens
Chocolate & the Chip is recalling Lavender chocolate chip cookies due to undeclared wheat, milk, and soy allergens found on product labels during a California Department of Public Health inspection.
Product
Chocolate & the Chip Lavender chocolate chip cookies: Cookies: 4 oz / 114 grams per pack. Cookies are packaged in uniform pairs in a food grade clear resealable bag and label Corrected Ingredients: Ingredients: All purpose flour (bleached wheat flour, malted barley flour…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0134-2022·2021-10-27
GE SIGNA Pioneer MRI Recall for Missing Image Slices
GE Healthcare is recalling 5 SIGNA Pioneer MRI systems where a software issue can cause missing image slices in 3D volume scans. This may lead to diagnostic gaps.
Product
SIGNA Pioneer nuclear magnetic resonance imaging system
Category
Medical Device
Distribution
19 states
ModerateFDA (Drugs)·D-0015-2022·2021-10-27
Coppertone Pure & Simple 50 Sunscreen Spray Recall for cGMP Deviations
Beiersdorf Inc. is recalling Coppertone Pure & Simple 50 Sunscreen Spray due to manufacturing practice deviations. Approximately 36,660 cans were distributed nationwide.
Product
Coppertone Pure & Simple 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02880 0
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0019-2022·2021-10-27
Rocuronium Bromide Injection Lacks Paralyzing Agent Warning
Piramal Critical Care is recalling Rocuronium Bromide Injection because the finished product vial lacks the required "WARNING: PARALYZING AGENT" statement on the flip cap. The missing warning could lead to unsafe use of this prescription neuromuscular-blocking drug.
Product
Rocuronium Bromide Injection 50mg/5 mL, 5mL Multi-Dose Vial, Rx only, Manufactured for: Piramal Critical Care, Bethlehem, PA 18017, USA, Manufactured by: Sanovel Ilac, San. Ve Tic. A.S. Istanbul, Turkey, NDC 66794-0228-41
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0120-2022·2021-10-27
Diagnostic Control Material Outside Expected Range, Potential for Delayed Results
Ortho Clinical Diagnostics is recalling VITROS Anti-SARS-CoV-2 Immunodiagnostic Controls that may be outside the expected control range, potentially delaying diagnostic test results in laboratory systems.
Product
VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Quantitative Controls (IVD)- For use in monitoring the performance of the VITROS ECi/ECiQ/3600 Immunodiagnostic Systems and the VITROS 5600/XT 7600 Integrated Systems when used with the VITROS Immunodiagnostic Products…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0022-2022·2021-10-27
AirDuo Digihaler 232/14 Inhalation Powder Subpotent Recall
Teva Pharmaceuticals is recalling AirDuo Digihaler 232/14 inhalation powder because some units do not deliver the correct amount of salmeterol as labeled.
Product
AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14 mcg) Inhalation Powder, Sample Not For Sale, Rx Only, Mktd by: Teva Respiratory, LLC, Frazer, PA 19355, Manufactured in Ireland, NDC 59310-530-08.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0025-2022·2021-10-27
AirDuo Digihaler 232/14 Inhalation Powder Recall for Subpotent Salmeterol
Teva Pharmaceuticals is recalling approximately 5,500 units of AirDuo Digihaler 232/14 inhalation powder distributed nationwide because some inhalers contain less salmeterol than the labeled dose.
Product
AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd by: Teva Respiratory, LLC, Frazer, PA 19355, Manufactured in Ireland, NDC 59310-136-06
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0143-2022·2021-10-27
Smith & Nephew cannulated screw label incorrectly indicates threading type
Smith & Nephew is recalling 6.5mm x 165mm cannulated screws because the product label incorrectly states the screws are fully threaded when they are actually partially threaded.
Product
6.5MMX165MM CANNULATED SCREW
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0017-2022·2021-10-27
Coppertone Pure & Simple Baby 50 Sunscreen Spray Recalled for cGMP Deviations
Beiersdorf Inc. is recalling 14,748 cans of Coppertone Pure & Simple baby 50 Sunscreen Spray due to cGMP (current Good Manufacturing Practice) deviations. The product was distributed nationwide.
Product
Coppertone Pure & Simple baby 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02881 7
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0026-2022·2021-10-27
Omeprazole Magnesium Acid Reducer Capsules Recalled for Staple Contamination
Dr. Reddy's Laboratories is recalling Acid Reducer (Omeprazole Magnesium) 20 mg capsules nationwide because staples have been found co-mingled with capsules in bottles.
Product
ACID REDUCER — ACID REDUCER (OMEPRAZOLE MAGNESIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0024-2022·2021-10-27
AirDuo Digihaler inhalation powder subpotent drug recall
Teva Pharmaceuticals is recalling AirDuo Digihaler 113/14 inhalation powder because some batches do not deliver the labeled amount of salmeterol, a critical active ingredient for asthma and COPD control.
Product
AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd. by: Teva Respiratory, LLC, Frazer, PA 19355, Manufactured in Ireland, NDC 59310-129-06.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0151-2022·2021-10-27
HemosIL Liquid Anti-Xa Assay On-Board Stability Issue Recall
Instrumentation Laboratory is recalling HemosIL Liquid Anti-Xa, a coagulation assay measuring heparin activity, due to reduced on-board instrument stability from 7 days to 5 days.
Product
HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative determination of unfractionated heparin (UFH) and low molecular weight heparin (LMWH) activity in human citrated plasma on IL Coagulation Systems, (ACLTOP¿ Family, ACL TOP Family 50 Seriest and ACL…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0149-2022·2021-10-27
Heparin Activity Assay Labeling Correction: Reduced On-Board Stability
Instrumentation Laboratory is recalling HemosIL Liquid Anti-Xa kits due to a labeling correction. The on-board stability window has been reduced from 7 to 5 days.
Product
HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative determination of unfractionated heparin (UFH) and low molecular weight heparin (LMWH) activity in human citrated plasma on IL Coagulation Systems, (ACL TOP¿ Family, ACL TOP Family 50 Seriest and ACL…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0126-2022·2021-10-27
Plastic Tenaculum Surgical Instruments Recalled for Unconfirmed Manufacturing Standards
Stradis Medical is recalling plastic tenaculum surgical instruments because the manufacturer cannot confirm they were produced in accordance with required design and manufacturing standards. Approximately 2,483 kits were distributed nationwide and to Canada.
Product
Tenaculum, Plastic
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0021-2022·2021-10-27
AirDuo Digihaler 113/14 Inhalation Powder Subpotent Drug Recall
Teva Pharmaceuticals is recalling AirDuo Digihaler 113/14 inhalation powder because some units contain less salmeterol than the labeled dose. The affected sample batch was distributed nationwide.
Product
AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14 mcg) Inhalation Powder, Sample Not For Sale, Rx Only, Mktd by: Teva Respiratory, LLC , Frazer, PA 19355, Manufactured in Ireland, NDC 59310-520-08
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0027-2022·2021-10-27
Lupin Imipramine Pamoate Capsules Recalled for Failed Dissolution Test
Lupin Pharmaceuticals is recalling approximately 1,902 bottles of Imipramine Pamoate Capsules 125 mg due to out-of-specification results in dissolution testing at the 9-month stability checkpoint.
Product
IMIPRAMINE PAMOATE — IMIPRAMINE PAMOATE (IMIPRAMINE PAMOATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0016-2022·2021-10-27
Coppertone Pure & Simple Kids 50 Sunscreen Spray Recalled for cGMP Deviations
Beiersdorf Inc. is voluntarily recalling Coppertone Pure & Simple kids 50 Sunscreen Spray due to current Good Manufacturing Practice (cGMP) deviations. The recall affects 70,320 cans distributed nationwide.
Product
Coppertone Pure & Simple kids 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02882 4
Category
Drug
Distribution
Distributed nationwide
ModerateCPSC·22008·2021-10-27
5.11 Tactec Plate Carriers Recalled Due to Injury Hazard
5.11 Inc. is recalling about 45,170 Tactec Plate Carriers (style 56100) because the cable in the quick release system can separate from the handle, preventing swift removal in an emergency. No injuries have been reported.
Product
56100 Tactec™ Plate Carriers
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0020-2022·2021-10-27
GlipiZIDE Extended-Release Tablets 2.5 mg Nationwide Recall
American Health Packaging is recalling GlipiZIDE Extended-Release Tablets 2.5 mg (Lot #194141) nationwide because dissolution test results exceeded specification, which may affect the drug's effectiveness.
Product
GlipiZIDE Extended-Release Tablets, 2.5 mg, 30 Tablets (3 blister cards each with 10 individually blistered doses), Rx only, Manufactured by: Patheon Pharmaceuticals Inc., Cincinnati, OH 45237; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054. Carton NDC#…
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·21V839000·2021-10-26
Nissan Recalls 2017-2019 Rogue Hybrid Vehicles for Engine Harness Defect
Nissan is recalling 2017-2019 Rogue Hybrid vehicles because contact with the ECM bracket may damage the engine harness, causing a blown fuse and potential engine stall.
Product
NISSAN — NISSAN ROGUE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21E090000·2021-10-26
WABCO Trailer ABS Systems Recalled for Brake Pressure Loss Risk
WABCO is recalling certain Trailer ABS Systems because improperly tightened screws may loosen, causing pressure loss and potential brake failure.
Product
SERVICE BRAKES, AIR recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V837000·2021-10-25
2020-2023 IC Bus School Buses Recalled for Engine Shut Down Risk
Navistar is recalling 2020-2023 IC Bus CESB school buses due to an engine control module defect that may cause unexpected engine shutdown while driving, increasing the risk of crashes and emergency evacuation situations.
Product
IC BUS — IC BUS CESB
Category
Vehicle
Distribution
Distributed nationwide