Crib & Bassinet Recalls

33 matching recalls in our database. Updated twice daily from CPSC, NHTSA, and FDA.

What this page covers

Recalls of cribs (full-size, mini, and portable), bassinets, bedside sleepers, and cradles — products intended as a sleep space for infants up to about twelve months old. We pull these from CPSC's official recall feed twice a day.

Why these products get recalled

The reasons repeat across the past decade:

Entrapment — a gap or opening that can trap an infant's head, neck, or limb. This was the failure mode that led CPSC to ban drop-side cribs in 2011.
Suffocation — soft, padded, or inclined sleep surfaces that don't meet the "firm and flat" requirement.
Fall and collapse hazards — weakened hardware that lets the bassinet tip or come apart.
Toxic content — lead in paint or finishes.

Federal safety standards apply: full-size cribs are governed by 16 CFR Part 1219, non-full-size cribs by 16 CFR Part 1220, bassinets and cradles by 16 CFR Part 1218, and bedside sleepers by 16 CFR Part 1236. Products that fail to meet these standards trigger a CPSC recall.

What to do if a recall affects you

Stop using the product immediately. Move the infant to a firm, flat surface in a different crib or bassinet.
Contact the manufacturer for the specific remedy — refund, repair kit, or replacement. The CPSC recall notice always lists how to do this.
Don't resell or give it away. The Consumer Product Safety Improvement Act prohibits resale of recalled children's products.
Register your crib or bassinet with the manufacturer so you're notified directly. CPSC also runs free recall email alerts at cpsc.gov/Newsroom/Subscribe.

Safe-sleep reminders

Independent of any specific recall: the American Academy of Pediatrics recommends a firm, flat sleep surface, fitted sheet only, no blankets, pillows, bumpers, or soft toys, and placing the infant on their back for every sleep until age one.

Recent recalls

Date	Source	Product	Brand	Severity	Units
2026-08-19	FDA Device	FDA Recall: GM Helix Implant, Endosseous Dental Implant Article No. 109.984	Straumann USA LLC	Class II	N/A
2026-08-12	FDA Device	FDA Recall: STRYKER PKG., STRYKEFLOW SUCTION/IRRIGATOR PS, Catalog Number 0250070540	Stryker Corporation	Class II	N/A
2026-08-12	FDA Device	FDA Recall: STRYKER PKG., SINGLE SPIKE TUBE SET, Catalog Number 0250070530	Stryker Corporation	Class II	N/A
2026-08-12	FDA Device	FDA Recall: STRYKER AHTO TUBE SET PACKAGING, Catalog Number 0250070600	Stryker Corporation	Class II	N/A
2026-08-12	FDA Device	FDA Recall: Happiest Baby, Inc Pre-loved SNOO Smart Sleeper Model:S1000	Happiest Baby, Inc	Class II	N/A
2026-08-12	FDA Device	FDA Recall: STRYKER AHTO DUAL SPIKE TUBE SET PACKAGING, Catalog Number 0250070640	Stryker Corporation	Class II	N/A
2026-08-12	FDA Device	FDA Recall: STRYKER AHTO TUBE SET WITH TIP PACKAGING, Catalog Number 0250070620	Stryker Corporation	Class II	N/A
2026-08-12	FDA Device	FDA Recall: Charger for the Therabody Theragun, G4 PRO massage device, and products which include the 4th Genera	Therabody, Inc	Class II	N/A
2026-08-06	CPSC	Play Yard and Crib Mattresses Recalled Due to Risk of Serious Injury or Death from Entrapment and Fire Hazards; Violate Mandatory Standards for Mattresses; Sold on Amazon by Voomf	Shanghaiyuejiuyaoguojimaoyiyouxiangongsi (Shanghai Yuejiuyao International Trade Co., Ltd.), dba Voomf, of China	N/A	2,401
2026-08-05	FDA Drug	FDA Recall: Azelaic Acid Gel, 15%, 50 gram tubes, For Topical Use only, Rx only, Distributed by: Glenmark Pharma	Glenmark Pharmaceuticals Inc., USA	Class II	N/A
2026-07-08	FDA Device	FDA Recall: Hillrom VOLARA System P.CIRCUIT 5KIT AC, (Single Patient Use Circuit), Model/Catalog Number REF M084	Baxter Healthcare Corporation	Class I	N/A
2026-07-08	FDA Device	FDA Recall: Hillrom VOLARA P.CIRCUIT 5KIT (System Single Patient Use Circuit), Model/Catalog Number REF M08270;	Baxter Healthcare Corporation	Class I	N/A
2026-07-08	FDA Device	FDA Recall: Hillrom VOLARA System P.CIRCUIT KIT (Single Patient Use Circuit), Model/Catalog Number REF M08085; O	Baxter Healthcare Corporation	Class I	N/A
2026-07-08	FDA Device	FDA Recall: Hillrom VOLARA System P.CIRCUIT KIT AC (Single Patient Use Circuit), Model/Catalog Number REF M08473	Baxter Healthcare Corporation	Class I	N/A
2026-05-20	FDA Device	FDA Recall: Brand Name: DONJOY Product Name: ICEMAN W/,UNIV,LOOP,NS,RH Model/Catalog Number: 11-1422 Software	DJO, LLC	Class II	N/A
2026-05-20	FDA Device	FDA Recall: Brand Name: DONJOY Product Name: ICEMAN CLASSIC CUBE Model/Catalog Number: 11-0494 Software Versi	DJO, LLC	Class II	N/A
2026-05-20	FDA Device	FDA Recall: Brand Name: DONJOY Product Name: ICEMAN W/,UNIV,LOOP,NS,EH Model/Catalog Number: 11-1424 Software	DJO, LLC	Class II	N/A
2026-05-20	FDA Device	FDA Recall: Brand Name: DONJOY Product Name: ICEMAN, W/COLDPAD, NS, RH Model/Catalog Number: 11-9099 Software	DJO, LLC	Class II	N/A
2026-04-16	CPSC	Generac Power Systems Recalls Portable Generators Due to Risk of Serious Injury or Death from Burn and Fire Hazards	-	N/A	149,400
2026-04-01	FDA Device	FDA Recall: Embrace Drill Tower, Wedged (25mm); Item Number: 645-081/62;	Waldemar Link GmbH & Co. KG (Mfg Site)	Class II	N/A
2026-04-01	FDA Device	FDA Recall: Embrace Drill Tower, Standard/Lateral (25mm); Item Number: 645-081/63;	Waldemar Link GmbH & Co. KG (Mfg Site)	Class II	N/A
2026-03-26	CPSC	AirClub Convertible Bassinets Recalled Due to Risk of Serious Injury or Death from Fall Hazard; Violates Mandatory Standard for Bedside Sleepers	Zhangzhou Qiangxing Supply Chain Management Co., Ltd. dba AirClub of China	N/A	110,400
2026-03-25	FDA Device	FDA Recall: Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion Leksell Gamma	Elekta, Inc.	Class II	N/A
2026-03-25	FDA Device	FDA Recall: Cub Pediatric Crib, Model FL19H	Stryker Medical Division of Stryker Corporation	Class II	N/A
2026-01-15	CPSC	Yixing Trading Recalls KEAWIS Crib Mattresses Due to Risk of Serious Injury or Death from Entrapment and Suffocation; Violates Mandatory Standard for Crib Mattresses	Yixing Trading of Richmond, Kentucky	N/A	1,500
2026-01-08	CPSC	The Kalencom Corporation Recalls SARO Braided Crib Bumpers Due to Risk of Serious Injury or Death from Suffocation; Violates Federal Crib Bumper Ban	The Kalencom Corporation, of New Orleans, Louisiana	N/A	55
2001-07-31	CPSC	CPSC, Fisher-Price Announce Recall of Portable Bassinets	Fisher-Price, of East Aurora, N.Y.	N/A	569,000
2001-06-14	CPSC	CPSC, KB Toys Announce Recall of Activity Gym Toys	KB Toys, of Pittsfield, Mass.	N/A	115,000
2000-08-23	CPSC	CPSC, Kids Line Inc. Announce Recall to Repair "Le Cradle" Bassinets	Kids Line Inc., of Los Angeles, Calif.	N/A	46,000
2000-06-05	CPSC	Infant Cargo Skirts Recalled by Associated Merchandising Corp.	The Associated Merchandising Corp. (AMC) of New York, N.Y.	N/A	9,500
2000-04-07	CPSC	CPSC, Fisher-Price Announce Recall of Infant Products	Fisher-Price, of East Aurora, N.Y.	N/A	105,000
2000-01-27	CPSC	In Wake of Second Death, CPSC and Burger King Again Urge Consumers to Destroy and Discard Pokemon Balls	Burger King Corporation	N/A	25
1999-12-27	CPSC	CPSC, Burger King Corporation Announce Voluntary Recall of Pokemon Ball	Burger King Corporation	N/A	25

Frequently asked questions

Are drop-side cribs still legal?▾

No. CPSC banned the sale, manufacture, and resale of drop-side cribs in 2011 under 16 CFR Part 1219 because of repeated entrapment and suffocation deaths.

Can I sell a recalled crib at a garage sale?▾

No. Federal law (the Consumer Product Safety Improvement Act) prohibits the resale of any recalled children's product, whether at a garage sale, online, or at a thrift store.

How do I tell if my specific crib is recalled?▾

Check the model number and date code on the label affixed to the crib against the recall notice. Manufacturers list the affected model and date ranges on every recall.

What's the difference between a bassinet and a bedside sleeper?▾

A bassinet is a standalone sleep surface. A bedside sleeper attaches to or sits flush against an adult bed. They're covered by separate federal standards (1218 for bassinets, 1236 for bedside sleepers).

Is co-sleeping safe in any product?▾

The AAP and CPSC recommend room-sharing without bed-sharing. Even products marketed as 'bedside sleepers' have to comply with the federal standard and the manufacturer's exact setup instructions to be used safely.

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Sources: CPSC (cpsc.gov), NHTSA, FDA. WatchRecall aggregates official government recall data; for original notices see the source link on each individual recall.