Hazard

Leakage recalls

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

What the numbers show

Total: 717
Critical: 4
Severe: 166
Most recent: 2026-08-26

Of the 717 leakage recalls we have scored against our rubric, 4 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 166 (23%) 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 leakage 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.

476–500 of 717

SevereFDA (Drugs)·D-1032-2017·2017-08-02
SCA Pharmaceuticals Recalls Potassium Chloride Injection Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of Potassium Chloride 20 meq in Sodium Chloride 0.9% injection due to a lack of assurance of sterility and potential for leaking.
Product
Potassium Chloride 20 meq Added to Sodium Chloride 0.9% 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0832-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1025-2017·2017-08-02
SCA Pharmaceuticals Recalls Phenylephrine HCl Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of Phenylephrine HCl 10 mg in 0.9% Sodium Chloride 250 mL bags because they may leak and lack assurance of sterility.
Product
PHENYLephrine HCl 10 mg in 0.9% Sodium Chloride 250 mL Bag, Preservative Free, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0811-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1002-2017·2017-08-02
SCA Pharmaceuticals Recalls Diltiazem Injection Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling Diltiazem 125 mg injection bags because they were made with recalled saline bags that may leak, compromising sterility.
Product
Diltiazem 125 mg in 0.9% Sodium Chloride, 1 mg per mL, Total Volume 125 mL Single Dose Container bag, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205 (877) 550-5059; NDC: 70004-0541-35.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1019-2017·2017-08-02
SCA Pharmaceuticals Recalls Epinephrine HCl Due to Sterility Concerns
SCA Pharmaceuticals is recalling Epinephrine HCl 4 mg in 0.9% Sodium Chloride 250 mL due to a lack of assurance of sterility and potential for leaking.
Product
EPINEPHrine HCl 4 mg in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0613-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1010-2017·2017-08-02
SCA Pharmaceuticals Recalls Fentanyl Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling fentanyl citrate syringes due to a lack of assurance of sterility and potential for leaking.
Product
fentaNYL as citrate 5 mcg/mL in 0.9% Sodium Chloride 1 mL in Single Dose syringe, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0225-24
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1031-2017·2017-08-02
SCA Pharmaceuticals Recalls Phenylephrine Injection Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of Phenylephrine 50 mg injection due to a lack of assurance of sterility and potential for product leakage.
Product
PHENYLephrine 50 mg in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0820-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1015-2017·2017-08-02
SCA Pharmaceuticals Recalls Fentanyl and Bupivacaine Infusion Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of fentanyl and bupivacaine infusion bags because they may leak and lack assurance of sterility.
Product
fentaNYL 2 mcg/mL + BUPIvacaine 0.125% PF in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0254-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1013-2017·2017-08-02
SCA Pharmaceuticals Recalls Fentanyl Infusion Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of fentanyl infusion bags because they may leak and lack assurance of sterility.
Product
fentaNYL 10 mcg/mL PF in Sodium Chloride 250 mL (Total Dose=2500 mcg), Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0229-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1007-2017·2017-08-02
SCA Pharmaceuticals Recalls Bupivacaine HCl Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling Bupivacaine HCl 0.2% bags because they may leak and lack sterility assurance.
Product
BUPIVacaine HCl 0.2% IN 0.9% Sodium Chloride 250 mL Bag Preservative Free (Total Dose Bupivacaine 500 mg per 250 mL), Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0066-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1005-2017·2017-08-02
SCA Pharmaceuticals Recalls Bupivacaine HCl Due to Sterility Concerns
SCA Pharmaceuticals is recalling Bupivacaine HCl 0.1% bags due to a lack of assurance of sterility and potential for leaking.
Product
BUPIVacaine HCl 0.1% PF (From 0.75%) in 0.9% Sodium Chloride, 250 mL Bag, Preservative Free (Waste From 250 mL Bag), Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0060-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1012-2017·2017-08-02
SCA Pharmaceuticals Recalls Fentanyl Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling fentanyl syringes because they may leak and lack assurance of sterility.
Product
fentaNYL 10 mcg/mL PF in NS 1 mL Fill in 3 mL syringe, Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0229-05
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1026-2017·2017-08-02
SCA Pharmaceuticals Recalls Phenylephrine IV Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of Phenylephrine 10 mg IV bags due to a lack of assurance of sterility and potential for leaking.
Product
PHENYLephrine 10 mg in 0.9% Sodium Chloride 250 mL bag, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 ---- NDC# 70004-0811-59
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1003-2017·2017-08-02
SCA Pharmaceuticals Recalls Magnesium Sulfate Injection Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling 40 bags of Magnesium Sulfate 4 g in 0.9% Sodium Chloride because they were made with recalled saline bags that may leak, compromising sterility.
Product
MAGNESIUM Sulfate 4 g added to 100 mL 0.9% Sodium Chloride, Total Approximate Volume 108 mL (does not include mfg. overfill) Single Dose Container bag, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205 (877) 550-5059; NDC: 70004-0737-32.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1022-2017·2017-08-02
SCA Pharmaceuticals Recalls Repinephrine Bitartrate Due to Sterility Concerns
SCA Pharmaceuticals is recalling Repinephrine Bitartrate 16 mg in 0.9% Sodium Chloride 250 mL due to a lack of assurance of sterility and potential for product leakage.
Product
NORepinephrine Bitartrate 16 mg in 0.9% Sodium Chloride 250 mL from Stock, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0775-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1033-2017·2017-08-02
SCA Pharmaceuticals Recalls Potassium Chloride Injection Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of Potassium Chloride 40 meq Added to Sodium Chloride 0.9% 250 mL due to lack of assurance of sterility and potential for leaking.
Product
Potassium Chloride 40 meq Added to Sodium Chloride 0.9% 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 ---- NDC# 70004-0833-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1004-2017·2017-08-02
SCA Pharmaceuticals Recalls Phenylephrine HCl Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling two bags of Phenylephrine HCl 10 mg in 0.9% Sodium Chloride because they were made with recalled saline bags that may leak.
Product
PHENYLephrine HCl 10 mg in 0.9% Sodium Chloride, (Final Concentration = 0.1 mg per mL), Total Volume 100 mL Single Dose Container bag, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205 (877) 550-5059; NDC: 70004-0810-32.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1034-2017·2017-08-02
SCA Pharmaceuticals Recalls Fentanyl and Ropivacaine Infusion Bags
SCA Pharmaceuticals is recalling specific lots of fentanyl and ropivacaine infusion bags due to a lack of assurance of sterility and potential for leaking.
Product
fentaNYL 2 mcg/mL + Ropivacaine 0.2% PF in NS 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0260-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1023-2017·2017-08-02
SCA Pharmaceuticals Recalls Phenylephrine HCl Injection Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of Phenylephrine HCl injection because the product lacks assurance of sterility and has the potential to leak.
Product
PHENYLephrine HCl 60 mg in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0809-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1017-2017·2017-08-02
SCA Pharmaceuticals Recalls Hydromorphone Syringes Due to Sterility Concerns
SCA Pharmaceuticals is recalling specific lots of Hydromorphone injection syringes because they may leak and lack assurance of sterility.
Product
Hydromorphone 0.5 mg/mL in 0.9% Sodium Chloride 1 mL Fill in 3 mL BD syringe, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0302-05
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1028-2017·2017-08-02
SCA Pharmaceuticals Recalls Phenylephrine Injection Due to Sterility Concerns
SCA Pharmaceuticals is recalling Phenylephrine 100 mg injection bags because they lack assurance of sterility and may leak.
Product
PHENYLephrine 100 mg in 0.9% Sodium Chloride 250 mL Bag, Rx only, SCA Pharmaceuticals 882PHENYLephrine 100 mg 1 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0813-40
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1001-2017·2017-08-02
SCA Pharmaceuticals Recalls CeFAZolin Bags Due to Sterility Concerns
SCA Pharmaceuticals is recalling 108 bags of CeFAZolin 3 g in 0.9% Sodium Chloride because the product was made with recalled saline bags that may leak, compromising sterility.
Product
ceFAZolin 3 g added to 100 mL 0.9% Sodium Chloride, Total Approximate Volume 115 mL Single Dose Container bag, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205 (877) 550-5059; NDC: 70004-0524-32.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0972-2017·2017-07-19
Baxter Recalls 5% Dextrose Injection Due to Sterility Concerns
Baxter Healthcare is recalling 54,528 bags of 5% Dextrose Injection because the bags may leak, compromising sterility.
Product
DEXTROSE — DEXTROSE (DEXTROSE MONOHYDRATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0973-2017·2017-07-19
Baxter Recalls Sodium Chloride Injection Bags Due to Sterility Concerns
Baxter Healthcare is recalling 295,200 bags of 0.9% Sodium Chloride Injection due to a lack of assurance of sterility and potential for leaking.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1883-2017·2017-05-03
CareFusion Recalls SmartSite Add-On Bag Access Device Due to Leakage
CareFusion is recalling 384,923 units of the SmartSite Add-On Bag Access Device because the spike port may separate or leak, potentially interrupting medication infusion.
Product
SmartSite Add-On Bag Access Device, Model No. 10013365
Category
Medical Device
Distribution
0 states
HighCPSC·17124·2017-03-30
humangear Recalls capCAP Bottle Caps Due to Burn Hazard
humangear is recalling capCAP bottle caps because they may leak or dislodge, posing a burn hazard when used with hot liquids. No injuries have been reported.
Product
humangear capCAP bottle caps
Category
Consumer Product
Distribution
Distributed nationwide