outdoor Recalls

134 recalls tagged with “outdoor”.

Health & Personal Care
HIGH
FDA DRUG

Major Pharmaceuticals Gabapentin 100 mg 10-Capsule Recall Nationwide 2025

Major Pharmaceuticals recalled Gabapentin Capsules, USP, 100 mg, 10 capsules per blister pack, distributed nationwide in the United States. The recall cites failed impurities and degradation specifications from routine stability testing, specifically an out-of-spec Highest Unknown Impurity. Consumers and healthcare providers should stop using this product immediately and contact The Harvard Drug集团

Gabapentin
Failed Impurities/Degradation
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Health & Personal Care
HIGH
FDA DRUG

Acuity Specialty Products Hand Sanitizer Recalled for Methanol Risk Due to Unperformed Component-LOT

Acuity Specialty Products recalled hand sanitizer products sold nationwide due to potential methanol presence. The recall covers Wyandotte, Sanifect E3 ethanol-based sanitizer products manufactured by AFCO. The issue stems from unperformed receipt testing on incoming alcohol components. Consumers and healthcare providers should stop use immediately.

Acuity Specialty Products
cGMP deviations:
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Food & Beverages
HIGH
FDA FOOD

Albertsons Store-Made Grilled Chicken & Basil Pasta Extra Large Recalled for Listeria (2025)

Albertsons Companies is recalling store-made Grilled Chicken & Basil Pasta Extra Large sold under Carrs-Safeway, Eagle and Safeway banners. The product contains a bowtie pasta ingredient recalled for Listeria monocytogenes contamination. It was distributed in AK, AR, AZ, CA, CO, HI, LA, NE, NM, NV, OK, SD, TX, UT and WY. Stop using the product and contact Albertsons for refund or replacement.

Albertsons
Listeria monocytogenes.
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Health & Personal Care
HIGH
FDA DRUG

Zydus Entacavir Recall 600 Bottles Over Impurity Degradation Issue (2025)

Zydus Lifesciences and Zydus Pharmaceuticals USA recall 600 bottles of Entacavir 1 mg tablets distributed nationwide in the United States. An out-of-specification organic impurity triggered the recall. Stop use immediately and contact a healthcare provider or Zydus for guidance.

Entacavir
Failed impurity/degradation
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Health & Personal Care
HIGH
FDA DRUG

ENTECAVIR Entecavir 0.5 mg Tablets Recalled Nationwide Over Impurity (2025)

Ent ecavir 0.5 mg tablets, distributed nationwide in the United States by Zydus Pharmaceuticals USA Inc., are recalled, affecting 912 bottles. The recall is due to an out-of-specification organic impurity detected in a batch, Class II. Healthcare providers and patients should stop using the product immediately and contact Zydus Pharmaceuticals USA for guidance.

ENTECAVIR
Failed impurity/degradation
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Health & Personal Care
HIGH
FDA DEVICE

BD BACTEC Blood Culture System Recall 1,086 Units Worldwide Over Unauthorized Access Risk (2025)

BD recalled 1,086 BD BACTEC Blood Culture System units worldwide after unauthorized access to product service credentials. The breach could compromise confidentiality, integrity and availability of affected devices and data. Hospitals and healthcare providers should stop using the device immediately and follow BD’s recall instructions.

BD
Product service
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Food & Beverages
HIGH
FDA FOOD

Black Sheep Egg Company Free Range Grade AA Eggs Recalled for Salmonella Risk (20,625 Dozen) 2025

Black Sheep Egg Company recalled 20,625 dozen eggs sold at retail and wholesale locations in Arkansas and Missouri after a potential Salmonella contamination. The eggs are Free Range Grade AA Large Brown, loose-packed in boxes. Consumers should not consume these eggs and should contact Black Sheep Egg Company for refunds or replacements.

Black Sheep Egg Company
Potential Salmonella
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Recalled Five Below Tabletop Fire Pit – smooth model
HIGH
CPSC

Five Below Recalls Tabletop Fire Pits for Risk of Serious Burn Injury

Five Below recalls two tabletop fire pits after reports of alcohol fuel flames jetting and spreading. The recall affects devices sold nationwide. Stop using the recalled pits immediately and contact Five Below for a refund. Full refunds available or $5 option; mail-back refunds possible with photo submission.

Five Below
Alcohol fuel
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Recalled IcyBreeze Buddy Portable Misting Fan in slate blue
HIGH
CPSC

IcyBreeze Recall Expands Over Fire Hazard Risk in Portable Misting Fans (2025)

IcyBreeze recalled the IcyBreeze Buddy portable misting fan due to a charging fire hazard. The recall affects consumers who own the IcyBreeze Buddy with a 1.5-liter water tank and a 10,000 mAh lithium-ion battery. Affected units must be returned for a full refund and disposal guidance. Call 817-900-2664 or visit the recall page to begin the process and receive a $150 credit at Solo Brands brands.

IcyBreeze Cooling
The misting
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Food & Beverages
HIGH
FDA FOOD

Taproom Gourmet 15lb Bulk Madison Mix Recalled Over Undeclared Allergens

Taproom Gourmet recalled 3,547 cases of 15lb bulk Madison Mix after undeclared allergens were found. The recall cites no ingredient label as the defect. Consumers should not consume the product and should seek refund or replacement from Egress Capital Partners Inc.

Taproom Gourmet
No ingredient
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Health & Personal Care
HIGH
FDA DEVICE

Baxter Healthcare Oral Probe Recalled for 5,209 Units Misconfigured as Rectal Probes (2025)

Baxter Healthcare recalled 5,209 oral/axillary probes used with Welch Allyn SureTemp Plus thermometers nationwide in the United States, Canada and Colombia. The probes were inadvertently programmed with the rectal configuration, which can yield a lower temperature reading. Healthcare providers and patients should stop using the affected probes immediately and follow Baxter’s recall instructions.

Baxter Healthcare
Affected oral/axillary
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Health & Personal Care
HIGH
FDA DEVICE

UIH Technologies uEXPLORER MD PET/CT Recall for 2 Units in 2025

UIH Technologies recalled 2 uEXPLORER MD PET/CT systems after finding third-party outer covers can trap between the patient table and gantry. The interference can occur during table movement. Hospitals and healthcare facilities should stop using the devices and await instructions from UIH Technologies LLC.

UIH Technologies
Third-party outer
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Health & Personal Care
HIGH
FDA DEVICE

GE Medical Systems Israel Recalls 11 Elscint Cardial Gamma Cameras in 2025

GE Medical Systems Israel recalls 11 Elscint Cardial dual-head gamma cameras used for cardiac imaging worldwide. The recall concerns detector mounting that could fail if the unit is moved without proper support. Hospitals should stop using these devices immediately and follow GE’s recall instructions.

GE Medical Systems Israel
GE HealthCare
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ultrasound L17-5 Transducer Recalled for Useful-Life Labeling (2025)

Two Philips Ultrasound L17-5 transducers distributed nationwide to hospitals are recalled. The recall targets labeling that defines the devices' useful life. Stop using the transducers and follow Philips Ultrasound's instructions. Hospitals should contact Philips Ultrasound for guidance.

Philips Ultrasound
To provide
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Tag Statistics

Total Recalls
134

Related Tags

chemical hazardpoisoning riskelectrical hazardstop use immediatelyreturn for refundfda regulatedcpsc regulatedimmediate actionadult productelderly producttoddler productnhtsa regulated