Hazard

Leaking recalls

181 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total: 181
Critical: 1
Severe: 38
Most recent: 2026-08-12

Of the 181 leaking recalls we have scored against our rubric, 1 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 38 (21%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all leaking recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

101–125 of 181

SevereFDA (Drugs)·D-0870-2017·2017-06-07
SCA Pharmaceuticals Recalls Morphine Sulfate Injectable Bags Due to Leaking
SCA Pharmaceuticals is recalling 80 bags of morphine sulfate injectable solution because the bags are leaking at the seam, compromising sterility.
Product
morphine sulfate in 0.9% Sodium Chloride injectable, 1 mg per mL, Total Volume 100 mL, Single Dose Container bag, (Total morphine Dose 100 mg/ 100mL), Preservative Free (Contains Sulfites), Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205, NDC 70004-0100-32.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0661-2017·2017-04-19
Akorn Recalls Latanoprost Ophthalmic Solution Due to Sterility Assurance Issues
Akorn, Inc. is recalling Latanoprost Ophthalmic Solution, 0.005%, because bottles were found empty, under-filled, or leaking, compromising sterility.
Product
LATANOPROST OPHTHALMIC SOLUTION, 0.005%, 125 ug/2.5 mL, packaged in 2.5 mL bottle, Rx only, Manufactured for: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-625-12
Category
Drug
Distribution
Distributed nationwide
HighCPSC·17128·2017-04-11
Teavana Recalls Flip Tumblers Due to Hot Liquid Burn Hazard
Starbucks is recalling Teavana Flip Tumblers because they can leak hot liquid, posing a burn risk. Consumers should stop using them and contact Starbucks for a refund.
Product
Teavana Flip Tumblers
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0988-2017·2017-01-18
ICU Medical Recalls Tego Connectors Due to Potential Leaking Risk
ICU Medical is recalling Tego Connectors due to a potential risk of leaking. The devices are used as accessories for vascular access in hemodialysis.
Product
Tego Connector, Item No. D1000, NM1000 The Tego¿ Needle Free Access Device is intended for use as an accessory to a vascular access device (catheter) used in Hemodialysis or as an accessory to an Intravascular Administration Set for the administration or withdrawal of fluids t
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0868-2016·2016-06-01
Teva Recalls Linezolid Injection Bags Due to Sterility Concerns
Teva North America is recalling 546 bags of Linezolid Injection due to potential leaking that compromises sterility.
Product
Linezolid Injection, 600 mg/300 mL Single use container bags (NDC 0703-9060-31), packaged in 10 x 300 mL Single Use Container bags per Box Pack (NDC 0703-9060-33), Rx only, Manufactured In Hungary By: Teva Pharmaceutical Works Ltd., Hungary, H-2100 Godollo, Tancsics M. ut 82 Hung
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1725-2015·2015-06-17
Abbott Alkaline Wash Recall Due to Cap Leaking and Crystallization
Abbott Laboratories is recalling Alkaline Wash cleaning solution for Abbott Architect analyzers due to product leaking from the cap and crystallization around the cap.
Product
Alkaline Wash, List number 9D31-20, a cleaning solution used by the Abbott Architect analyzers. It is supplied in 500 mL bottles and contains NaOCl, NaOH, and KOH. It is shipped and stored at room temperature and is shipped ready to use.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1472-2015·2015-04-29
Churchill Medical Systems Recalls 8 Inch Standard Bore Extension Sets
Churchill Medical Systems is recalling 8-inch Standard Bore Extension Sets due to a potential leak caused by insufficient bonding between the needleless device and the female luer.
Product
8" Standard Bore Ext Set, Product Code: BN-481 Accessory device used to administer medical fluids
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1476-2015·2015-04-29
Churchill Medical Systems Recalls Bifurcated Sets Due to Leaking Risk
Churchill Medical Systems is recalling 1,050 bifurcated sets with check valves and Bionectors due to a potential for leaking caused by insufficient bonding.
Product
Bifurcated set with check vales and Bionectors, Product Code: BN-2082CV Accessory device used to administer medical fluids
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1478-2015·2015-04-29
Churchill Medical Systems Recalls 6-inch Trifurcated Sets with Bionectors
Churchill Medical Systems is recalling 1,650 6-inch trifurcated sets with Bionectors due to a potential leak caused by insufficient bonding between the needleless device and the female luer.
Product
6" Trifurcated set with Bionectors, Product Code: BN-944 Accessory device used to administer medical fluids
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1473-2015·2015-04-29
Churchill Medical Systems Recalls 7-Inch High Pressure Sets Due to Leaking Risk
Churchill Medical Systems is recalling 129,500 units of 7-inch High Pressure Sets with Bionector due to a potential for leaking caused by insufficient bonding.
Product
7" High Pressure Set with Bionector, Product Code: CMS-808 and CMS-808-1 Accessory device used to administer medical fluids
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1474-2015·2015-04-29
Churchill Medical Systems Recalls 7-Inch High Pressure Extension Sets
Churchill Medical Systems is recalling 6,850 units of 7-inch Standard Bore High Pressure Extension Sets due to a potential leak caused by insufficient bonding between the needleless device and female luer.
Product
7" Standard Bore High Pressure Ext Set, Product Code: CMS-809 Accessory device used to administer medical fluids
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1475-2015·2015-04-29
Churchill Medical Systems Recalls 7-inch High Pressure Extension Sets
Churchill Medical Systems is recalling 6,850 units of 7-inch Standard Bore High Pressure Extension Sets due to a potential leak caused by insufficient bonding.
Product
7" Standard Bore High Pressure Ext Set, Product Code: CMS-809 Accessory device used to administer medical fluids
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1477-2015·2015-04-29
Churchill Medical Systems Recalls 4-inch Trifurcated Sets Due to Leaking Risk
Churchill Medical Systems is recalling 2,650 units of 4-inch trifurcated sets with Bionectors and check valves due to a potential for leaking caused by insufficient bonding.
Product
4" Trifurcated set with Bionectors and check valves, Product Code: BN-3082CV and BN-3083CV Accessory device used to administer medical fluids
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1468-2015·2015-04-29
Churchill Medical Systems Recalls Bifurcated Extension Sets Due to Leaking Risk
Churchill Medical Systems is recalling 100 Bifurcated Extension Sets because a defect may cause leaking. The sets are used to administer medical fluids.
Product
Bifircated Extension Set, Product Code: BN-828 Accessory device used to administer medical fluids
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1469-2015·2015-04-29
Churchill Medical Systems Recalls 4-inch Microbore Double Lumen Sets
Churchill Medical Systems is recalling 2,350 units of 4-inch Microbore Double Lumen Sets due to a potential leak caused by an insufficient bond between the needleless device and the female luer.
Product
4" Microbore Double Lumen Set with Bionector, Product Code: BN-208 Accessory device used to administer medical fluids
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1471-2015·2015-04-29
Churchill Medical 4-inch Microbore T-Port Set Recalled for Leaking Risk
Churchill Medical Systems is recalling 450 units of 4-inch Microbore T-Port Sets due to a potential leak caused by insufficient bonding between components.
Product
4" Microbore T-Port Set, Product Code: BN-448 Accessory device used to administer medical fluids
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1470-2015·2015-04-29
Churchill Medical Systems Recalls 4-inch Microbore Trifurcated Extension Sets
Churchill Medical Systems is recalling 2,200 units of 4-inch Microbore Trifurcated Extension Sets due to a potential leak caused by insufficient bonding between the needleless device and female luer.
Product
4" Microbore Trifurcated Ext set, Product Code: BN-308 Accessory device used to administer medical fluids
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1467-2015·2015-04-29
Churchill Medical Systems Recalls 6-Inch Trifurcated Extension Sets for Leaking Risk
Churchill Medical Systems is recalling 5,200 6-inch trifurcated extension sets due to a potential leak caused by insufficient bonding between the needleless device and female luer.
Product
6" Trifurcated Extension Set, Product Code: AMS-375-1 Accessory device used to administer medical fluids
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1277-2015·2015-03-25
US Infusion Recalls Medstream IV Sets Due to Leaking
US Infusion is recalling 62,700 Medstream IV infusion sets because they may leak at the Y site. The sets were distributed in six states.
Product
Medstream 81" (206 cm) 20 drop Universal Administration Sets. Disposable IV infusion set with 3 year expiration date.
Category
Medical Device
Distribution
6 states
ModerateFDA (Drugs)·D-0045-2015·2014-11-05
Gilead Recalls Emtriva Oral Solution Due to Defective Leaking Containers
Gilead Sciences is recalling 6,290 bottles of Emtriva Oral Solution because the containers are defective and leaking around the cap.
Product
EMTRIVA — EMTRIVA (EMTRICITABINE)
Category
Drug
Distribution
1 state
ModerateFDA (Drugs)·D-0010-2015·2014-10-15
VistaPharm Recalls Metoclopramide Oral Solution Due to Leaking Containers
VistaPharm is recalling 322,650 cups of Metoclopramide Oral Solution because the containers leak when inverted.
Product
METOCLOPRAMIDE ORAL SOLUTION, USP 5 mg/5 mL, (present as the hydrochloride), 10 mL cups, Rx only. Manufactured by VistaPharm Inc., Largo, FL 33771. NDC 66689-031-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1615-2014·2014-10-08
Sagent Recalls Zoledronic Acid Injection Due to Sterility Concerns
Sagent Pharmaceuticals is recalling 10,622 bags of Zoledronic Acid Injection because of a lack of assurance of sterility and leaking premix bags.
Product
ZOLEDRONIC ACID — ZOLEDRONIC ACID (ZOLEDRONIC ACID)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0813-2014·2014-01-29
Churchill Medical AMS-530 Microbore Extension Sets Recalled for Leaking
Churchill Medical Systems is recalling AMS-530 Microbore Trifurcated Extension sets because a defective component may cause the sets to leak.
Product
AMS-530 7 Microbore Trifurcated Extension sets Product Usage: Intravascular administration set.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0694-2014·2014-01-15
ICU Medical Recalls NanoClave Needlefree Connectors Due to Potential Leaking
ICU Medical is recalling specific lots of NanoClave Needlefree Connectors because a small percentage of devices may leak.
Product
7" (18 cm) Appx 0.33 ml, Smallbore Ext Set w/NanoClave", Clamp, Rotating Luer, Part No. A1000, Item No. K7103-001 The ICU Needleless Connector is a single use, sterile, non-pyrogenic device intended for use as an accessory to intravascular administration set for the administr
Category
Medical Device
Distribution
14 states
SevereFDA (Devices)·Z-0683-2014·2014-01-15
ICU Medical Recalls NanoClave Needlefree Connectors Due to Potential Leaking
ICU Medical is recalling NanoClave Needlefree Connectors because a small percentage of devices may leak. The affected units were distributed worldwide.
Product
7" (18 cm) Appx 0.26 ml, Smallbore Ext Set w/MicroClave¿ Clear, NThe ICU Needleless Connector is a single use, sterile, non-pyrogenic device intended for use as an accessory to intravascular administration set for the administration of fluids to a patient through a cannula place
Category
Medical Device
Distribution
14 states